That hurricane was a dud for us, as I hope it was for you. We sat up late, anticipating every disaster on the forecasts, and ended up hiding in the basement for awhile, kind of like a campout. We finally went to sleep, wondering what kind of earth we'd awaken to find on Sunday.
The world was surprisingly calm on Sunday morning. But not my stomach. Oh no. Sicksleep went into double mode, probably because I'd had the audacity to keep chemo from stealing Saturday. I would pay that price dearly. Sunday and Monday were horrible days I hope never to repeat, so bad that by Tuesday I needed to head to Penn for IV drip to stave off dehydration. Mercifully, they also added Ativan, which is a nausea reliever as well as a sedative. The Ativan did its work well. However, just before I passed into oblivion, Dr. Fox and Lorelei came to visit. I tried so hard to focus on what they said. I could understand the words, but not what Dr. Fox was trying to tell me. I kept repeating, "Well, that's good, right? That's good?" And Dr. Fox wasn't specifically answering that, but instead telling me more. I suppose he's used to talking to a functional brain, and I didn't have one at that moment. At the end, this is what I finally understood:
The first time I had my CT scan, on June 12, the cancer was so involved in my liver, and my surrounding lymph nodes were so swollen with it, the contrast dye could not seep past it to fill the remainder of my abdomen. Therefore, that scan did not show a complete picture. Now, my lymph nodes are significantly shrunk, as are the tumors, so the contrast had no trouble reaching all areas of my abdomen. Obviously this is a huge positive result, and yes drugged Michelle, that's good, right. Dr. Fox just wanted to let me know that he now wants another CT scan in a month, so he can compare two complete scans. All I wanted to know was whether I could still switch to oral chemo, or if I would be forced to endure Ixabepillone for another cycle. Somehow I failed to get that answer.
The hydrated and improved me/I was going to return to Penn on Wednesday for my scheduled appointment, but it seemed foolish when I had just seen Dr. Fox the previous day. I talked to the scheduler about it, and we agreed. She left a message for Lorelei, who sounded exhausted when she reached me hours later. Not only that, but Lorelei was also unclear about the chemo switch. She would need to discuss it with Dr. Fox the next morning. Which was when I posted to Facebook that I would update the next evening. Unfortunately, somehow I missed Lorelei's Thursday message, and had nothing to report last night.
I finally got the news from a nurse this afternoon, just as my father and Libby were entering my house, fresh from Florida. The nurse told me, drum roll, I AM switching to oral chemo! The prescription is ready to be filled, but I should not fill it until next week when I talk to Lorelei. I will take it 7 days, and then skip it 7 days. I don't return to Penn until later this month. Thank goodness! This is not just about the chemo, either. I've been in the classroom much of this week, and I can't express how excited I am about this new school year, and new 6-year-olds. This chemo allows me that side of my life. It returns my weekends to me, my life, my choices.
So many people pray for me, it's extremely humbling. I have to believe that all these prayers are floating along the right passages to make a positive difference. You're all so filled with love and kindness, with such generous spirits, your prayers may be riding on a faster wave. I'm lucky to have you on my side. So extremely lucky.
Friday, September 2, 2011
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2 comments:
Michelle, GREAT NEWS!!!!! I'm excited for you and so happy for the positive note!!! XOXOXOXOOXO Thank you for keeping us all informed even when you're not feeling so great! I look for your posts! XOXO
Totally and completely awesome Michelle!! Have a great school year! Love, Rebecca
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