I'm a procrastinator, but I'm not a complainer. On the surface, the two traits seem completely unrelated, so I will relate them for you. I did not procrastinate writing in this blog, I simply had so little to say that would not sound like a complaint, I couldn't bear to type anything. I abhor complaining, frankly. If you're in my life, you either do not do it much, or you're my mother. Now, with actual potential on the horizon, I feel freer to let loose and share the shit. And then I can get to the good part :)
The truth is, life like this sucks. Ixebipillone or however you spell this chemo drug's name is horrible, creepy stuff. It starts off fine, and then it sneaks into your cells and bones and brain. With happy prednisone to counteract its ill effects, this chemo bestows a slow and deceptive descent. However, the prednisone vanishes, fewer pills to take each cycle, and insidious Ixebipilone roars forward into my veins and steals my life. The last few weeks have been increasingly miserable. It begins with a frustrating five hours a week in the chemo suite. The actual chemo drip is three hours, but there's always a long delay getting up to the suite from the pharmacy. By late the next day I can't eat, I have to eat, I stare at the refrigerator, everything inside smells terrible. I want to retch, as always, but it's useless, as always. My drip is on Wednesday, when I feel good. Thursday I decline ever so slightly. By Friday at noon I'm holed up somewhere in my house, completely incapacitated. It lasts and lasts. I see my visitors' belongings, but mostly I can never make my mouth move enough for a conversation and end up left alone with a view of a fancy purse. I can't sit up, therefore I can't use the computer. I drool, pass all kinds of gas. Feel tempted to drink less because going to the bathroom requires Herculean effort. I taste ... something. Something unkind, unwelcome, unidentifiable. My fingers and toes tingle, my feet freeze as the rest of my body perspires. Each week it lasts longer, takes over more of my days. Each week a new surprise. Like the hideous blood clot that passed from my sinus to my mouth on Sunday, that I coughed out onto my finger of all things. I started to ponder life with no quality of life, watching people I love grow increasingly nervous and sad. What's to be done about that?
Despite all this, I decided to go back to my first grade teaching position in September, blessed by the understanding principal who would let me take a half day off each week to go for chemo. It was insane to consider I could do it with just determination, so I was stockpiling other options to present to Dr. Fox today.
Armed with a complete cache of ammunition, I didn't kill myself or idiot drivers during my mad rush from New Teacher Orientation to Perelman's 3rd floor in 32 minutes, and it was with profound relief that I identified Jill sipping coffee in the waiting room. I should've taken it as a sign of things to come when I loudly announced to the somber waiting room, "Oh, my sister is here! I'm so happy my sister is here!" The phlebotomists are always informative. I could hang with them. Today, mine gave me lots of ideas for getting foood in on the bad days, which was helpful. Next stop, Lorelei the NP. I presented my litany of complaints and was prepared to ask for this med or that med or a blood transfusion to help me get more energy. Before I had the chance, Dr. Fox peeked in, and Lorelei excused herself to the hall to talk to him. She had already told me my blood and bilirubin counts continued to be at healthy levels.
Ten minutes later, an unsmiling Dr. Fox entered with two medical students and Lorelei. Was he worried, or being extra professional for the sake of the students? Lorelei had briefed him about my side effects, and he asked me to jump on the table for an exam. He felt all around my abdomen, then had the students do the same. I sat up as he presented my case history clinically for them, all facts included and correct. He reminded me that I would be having today's treatment and next week's, and then the CT scan a week later to determine the effectiveness of icky Ixabipillone. Yes, yes. "We really just need the scan to verify what we already know," Dr. Fox said. I gaped at him, holding my breath. "Obviously it's worked tremendously. That cancerous lymph node is gone, and everything looks and feels good. So I want to change your chemo." I breathed. This was turning into good news. It was just the beginning:
The new chemo is oral. I'll take my chemo pill each day, without side effects like nausea or exhaustion. My hair will stop falling out and what I've lost so far will grow back. I'll be able to be fully engaged in teaching first grade instead of figuring out how to make it tolerable. I'll feel just like me, with my real quality of life. I'll go on my cruise and dance badly. I won't need a wig. I'll set aside my handicapped placard. I'll visit Dr. Fox once a month for a blood draw and an update. I wanted to cry from the relief. I wasn't counting on an open window, or any sort of escape from prison. I just wanted out of solitary, and I was being handed my whole life. I was suddenly a non-evil, non-child killing Casey Anthony. I asked a few questions, the last among them whether I could hug him. So we hugged. Once Dr. Fox and his team were gone, the tears began to build as the full impact of chemo pill reached my taxed little brain. As I reentered the waiting room, realizing I was going to tell Ken and my mother and this blog this news, I started to bawl, making quite a spectacle of myself. A nurse came from the back, and I loudly announced to her and the nervous waiting room, "I'm so happy!" She gave me a hug, and then the receptionist came to join the party. Everyone was smiling.
I'm proud to have made a few people shed tears of joy over this news today. I'm back. I'm me. I'm going to get strong inside and out, feed my body the best foods on earth, and do whatever Dr. Fox wants me to do. Maybe my weird fortune cookie from last night didn't offer such an outlandish prediction: "You will live a long and heathy life." Just maybe.
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11 comments:
I can't begin to tell you how happy I am at the good news! Happy, but not surprised. I have never stopped believing in you. You are my hero and I am so proud of how you are handling this.
"I am so happy"
What great news. Yay you!!
CONGRATULATIONS on the fabulous news. I'm so happy for you. I guess our prayers are working. Love you Michelle, you are a fighter and don't forget that.
Michelle,
What wonderful news.Go out there and enjoy!
Francine Jackel
This is the best news ever!!!!!!!!! I am so happy to hear!!!!!! Xoxoxoxoxoxoxo
So happy to hear the wonderful news. I am so glad you will be able to go back to teaching. I know it makes you so happy. Keep on going. You are an inspiration to us all.
Best news I've heard in a very long time...thank you!
How wonderful. I can't wait to tell Zac (he's still asleep). I am looking forward to seeing you.
Debbie
I am so happy for you Michelle. You are a true Warrior!!
Michelle, I am so happy for you. Sad that the damn beast returned but thrilled that you have TKO'd it once again. Congratulations on your return to teaching. You deserve all good things and I think your fortune cookie is a good sign!
Hugs to sweet lady!
Beth P
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