Surgery day was a longer day than expected. We left the house at 4:15am to be sure we arrived at the hospital by 6:45. I’m glad we got there early, because the presurgery waiting room filled quickly. I was taken back in the 1st group, dressed in my hospital gown, and then joined by Bill. We met the anesthesiologist, and the surgeon who would be assisting my surgeon. Then my surgeon and a nurse practitioner came in to make 1cm marks up my entire leg, and measure the width at each mark – these measurements were used to determine the amount of chemo used in the procedure. Things were running late for me, but I think I was wheeled out after 9:00am. Once I arrived in the OR they got right to business, and I didn’t even realize that I was being given anesthesia until I started drifting away. That’s the last I remember till sometime close to 10:00pm that night. Previously, we had been told that the surgery would take 4-5 hours, but a family waiting room attendant told Bill that she had seen them go 5-7 hours. Since my surgery was done around 6:30pm, I guess I was one of the longer ones. Bill didn’t get to see me till 10:00pm (almost 18 hours since we left home that morning). Because they were out of beds, I stayed in recovery till the next day.
Friday, the first day after surgery, I was finally moved to a room on a vascular floor. I had a great deal of pain in my big toe, and a lack of feeling in my foot (except for pain), which had them concerned. They took an x-ray which showed evidence of rheumatoid arthritis or gout. I had to explain multiple times that I had no history of either. They had another specialist check me (a rheumatologist, I think), who said that it was not gout, and had her perplexed too. Once we got my foot down off the bed, some color, circulation, and feeling returned. My big toe and foot continued to be a source of pain, but no longer the concern it was. My foot was continually checked and showed a strong pulse, and my calf muscle was soft, another good sign. Both incisions were doing well.
Saturday was just another day of meds, vital sign checks, and moving out of the bed into a chair. Sunday included a physical therapist visit and learning how to use a walker. I didn’t really start to take steps till Monday. By then, we had played with the pain meds enough that I was beginning to have periods of relief and good rest. I still had no appetite at all, and some foods had a weird taste (don’t know if that’s a result of the chemo leaking, or side effect of the meds). I was also taking Prilosec and Zofran to help my stomach feel better (just slightly nauseous). At some point, the nurse wrote goals on my board: manage pain, and gain mobility.
On Tuesday, after proving I could empty my bladder and use the walker to move around the room, I was scheduled for discharge. I took a shower, which felt wonderful, though exhausting, and Bill helped me get dressed. We received discharge instructions, and I was wheeled out of the hospital with Bill carrying my new walker.