Well, I just had breakfast, and got dressed without too much difficulty. Still haven't managed a BM, but I haven't been eating that much either, so that will probably happen soon now that I'm home and on a more normal diet. I'm taking my stool softeners and extra fiber, so just letting nature take it's course. I had the spinal with sedation for my anesthetic and that worked really well. Didn't have any of the groggy headed feeling of GA and the effect lasted for several hours. They tried me on 10/325 hydrocodone after surgery and that didn't take care of the pain, which brings me to my first question for this group. What is a realistic level of pain? They asked me what my pain goal was and I said I didn't want to go higher than a 4. Was that too rosy? Anyway, my pain was spiking up around 7 and the nurses were giving me a hard time about more medication. On top of the pain issue I had a nurse had obviously hadn't been trained to work with hip replacement patients. She was about as gentle as a lady wrestler. She set me on a regular sized toilet which was too low, with toilet paper out of reach, aid cord out of reach and then left me there. I finally dragged myself up onto my walker and got myself into bed. This was on the first post op day. By the time my husband arrived for the day, by pain was spiking up around 7-8 and I was in tears. Since I'm not normally a teary person, he was understandably concerned. I ended up with a different potty nurse, and got put on a pain pump with Dilaudin? for 24 hours. That got the pain issue much better, but I still insisted on something stronger the the hydrocodone. I've been taking 10/325 oxycodone and that seems to be working pretty good. However, this brings me to my very strong recommendation for future patients who have to have multi-day hospital stays.
Know what pain medication you are on and keep track of when your last dose was.
I know that nurses are very busy and do the best they can, but unfortunately patients can get lost in the process. I thought that they had some kind of tracking system, but in my situation that didn't seem to be the case. The first time I was off the pain pump I had to call to remind them that I was due for pain meds. It still took over an hour for someone to show up. They were apologetic of course, but in the meantime my pain had a chance to spike again. After that I made to sure to note the time when meds were given and when the next was due. Then I called when the next was due. This took me through discharge with much less hassle.
After all that I have to say that I strongly agree with the advisors here that it is important to stay on top of the pain. I didn't start making real progress in getting around until I was on a regular med schedule. I'm setting my alarm so I make sure I take my oxycodone every four hours. I'm not going to worry about reducing the dose or lengthing the time between doses until I'm ready. Since I feel like I'm making pretty good progress, that shouldn't be more than another day or two. OK, enough sermonizing to now, I need to stretch a little and then take a little nap. My husband is such a worry wart about taking care of me, and I'm starting to worry about him. I'm sitting here in my office at the computer, and he's taking a nap on the floor right behind me so that I don't try to get up from my rolling chair without help. I'll try to write again later since I'm starting to feel a little fuzzy.