I am finally getting back here, and I apologize for the length of this post. I'm a 72 year old female. My decision to have knee replacement was complicated since I was having barely any knee pain. My pain was in my left butt area (duration 8 months) and I thought I needed a hip replacement on the left hip (felt like what I only imagine is bone-on-bone pain, when bending or after sitting). Well, the pain from recovery of knee surgery has made me forget all about any butt pain. When I'm not in pain, I'm fighting nausea from the oxycodone. I thought the oxy wasn't helping me at all, so yesterday I decided to stop it. But I was completely unable to sleep last night due to knee pain, so I took 5 mg at midnight. Took another 5 mg at 1:30. Another 5 mg at 4:45. Maybe got some sleep. So now the payback is wondering when I'm going to lose my breakfast. My plan is to take oxy only for sleeping. And try to only take 5 mg at bedtime, and maybe another 5 if I can't go back to sleep after the wake-up nightly pee-time.
I've gone to my knee surgeon for several years, getting cortisone injections here and there. No cortisone from Aug. 2018 until February 2021 when I injured my knee carrying a heavy log carrier into the house. At the time, my husband was newly diagnosed with Hodgkins's Lymphoma (transformed from CLL) and there was NO time for me to have any physical issues. So this knee surgeon gave me a cortisone injection but took new x-rays which showed extreme bone-on-bone arthritis. So why did I never feel it? I told him about the hip pain (I had a right hip replacement in November 2020, and that hip didn't show arthritis in the x-rays, it was necessary to do an MRI). His hip doc had refused to order an MRI so the hip surgery was done at a different hospital with a different ortho practice.
He said we would get through this with cortisone every 3 months. I was doing care for my husband round-the-clock - taking him several days a week for blood draws, him incontinent in a wheelchair, learning the ropes of navigating all that, having palliative care, helping him several times during the night. Then he came home from another hospitalization on hospice so family could finally have in-person visits after the past cold winter months of isolation. The hope of him getting a port for chemo/antibody treatment was over. His blood was not improving, no matter how many infusions he got. He passed away peacefully March 18. He never had pain, just extreme shortness of breath from his anemia.
On March 26, amongst myriad appointments with lawyers, banks, probate, etc., I had my surgery consultation and once again, the knee doc said no to any investigation into my hip pain. He thinks it is related to the knee and once the knee is strong the hip pain will resolve. Maybe he's right. Either way, the knee looked horrible in his x-ray, so I also thought "well, maybe if I need another hip replacement, the strong new knee will offer the new hip a better support for it's recovery if I need it done."
So here I am. I took the earliest surgery date he could give me, which happened to fall on my birthday! The hospital brought he chocolate cake on my lunch tray! And up it came a few hours later, I assumed my nausea then was due to general anesthesia, which I had never had before. I stayed in the hospital one night due to the nausea and urinary retention. My dear son is living with me until I don't need his help any longer. He is able to work from home. It is a major blessing having him here.
So as I said in my earlier post, my physical therapist thinks I can stop the oxy and don't need a walker either. She is happy with my progress with ROM but is concerned about the nausea. No fevers, vitals are always fine. I took hydrocodone with my hip replacement and had no problem with nausea. So I wonder if now is the right time to tough things out with just tylenol during the day and oxy at night only. Or should I call my doc and see if they recommend another drug strategy.
I have a wonderful ice machine thing that works great and I'm spending time every day laying in bed with more elevation. The swelling has noticeably decreased in the last day or so.
I'm glad you all are here. I've learned a lot from the sticky messages and topics. And now it's time for my shower! Yes, a highlight of the day!