Back to the cancer center. This time I dressed a little nicer and carried a lighter bag. I was starting to realize what a time consuming thing it was to have cancer.
Today we would be accessing the IP (intra-peritoneal) port under my left breast for the first time to administer Cisplatin, the anti-cancer drug, directly into my abdominal cavity where the tumor had been removed. We would also be accessing the chest port at the same time to administer fluids and anti-nausea medicine.
Whereas yesterday I sat in a recliner, today I was in a bed (which was actually more like a gurney). This was so that when the Cisplatin was administered I could rock back and forth to coat the area where the cancer had been. It sounds more exciting than it really was.
I had been told that today would be a longer day, as in seven to eight hours of chemo. I was pleasantly surprised that I was done in only three.
I had also heard all about the horrible side effects of Cisplatin: abdominal bloating and cramps, nausea, vomiting, and upset stomach. The nurse told me that the nausea usually took a day or two before it showed up.
The nurse took a lot of time to explain everything she was doing, and she gave some great advice about handling the nausea. There were no immediate side effects this time, like there had been with the Benadryl and the restless leg syndrome the day before.
Before we were done, the nurse saw that my CA 125 test results were in from yesterday’s blood work. The CA 125 is “a protein that is a so-called tumor marker or biomarker, which is a substance that is found in greater concentration in tumor cells than in other cells of the body. In particular, CA 125 is present in greater concentration in ovarian cancer cells than in other cells” (courtesy of medicinenet.com).
The night before my surgery my CA 125 was over 450. The current test showed the level was now 37 before I’d even had my first chemo treatment. The nurse was amazed, saying they rarely see numbers that low before the first chemo treatment. The norm is anything below 35, so it was definitely a good number.
As we were leaving the center after chemo, I ran into my oncologist coming from the hospital. She had seen my number, had already called to tell my family physician the good news, and was ecstatic. She actually said that we had a good chance of “curing” my cancer. The word “cure” is not one you hear very often when speaking of cancer. It was the best thing she could have told me.
Jut like yesterday, I felt pretty good after chemo. My daughter, Dominique, and my son’s girlfriend, Nicole, took me to Target and Buffalo Exchange for some shopping. Other than feeling fatigued, I ate a good dinner and thought to myself: maybe it won’t be as bad as everyone keeps saying it will be. I slept well and hoped for the best.
The next morning, Saturday, I woke up and felt a little tired and queasy, but nothing too extreme. By lunchtime I felt nauseous. Really nauseous. And nothing helped. It got progressively worse as the day wore on.
I took the anti-nausea meds the doctor had prescribed (Zofran and Compazine), but really didn’t notice that they helped all that much. The Compazine made me feel woozy and drunk. All I could do was stay in bed and not move. The slightest movement made me feel nauseous.
The entire weekend was a battle. I was too nauseous to eat, but I knew that not eating and having an empty stomach would only make the problem worse. I ate some crackers and tried to drink water. I wasn’t used to being in bed all day, and being so inactive was driving me crazy. On top of that, the Cisplatin made me feel like there was electricity coursing through my body, so trying to stay still was impossible. My friends Liz and Todd came over to see what they could do.
Sunday was even worse. I had constant nausea and felt restless, anxious, and like I had lost all control over what was happening to me. If you’re the type of person, like me, who is very active and doesn’t even like to take an aspirin, having your body pumped full of poison is not an easy thing to go through. I thought I would first go mentally crazy, and then the chemo drugs would kill me off after that.
I ate nothing more than a small amount of white rice, more crackers, and drank water and Gatorade. The nausea was so bad that putting anything in my mouth, even water, made me gag.
Nicole, bless her heart, cooked dinner for the rest of the family. Within ten minutes of starting dinner I had to run to the back of the house to escape the smell. Within another two minutes, when the scent of sauteed garlic and onions wafted into the bedroom, I had to sprint to the bathroom. Once again, my stomach was empty. She felt horrible for not realizing how sensitive I was to strong smells, I felt bad for her for feeling so bad, and we opened all the doors to air out the house.
After dinner we all drove to Liz and Todd’s house. I needed the fresh air and a distraction from feeling like I was going to jump out of my skin. The house was starting to feel like a prison. It was great to see good friends and it took my mind off feeling so horrible. When we left, though, I was so weak and out of it, I almost passed out when I stood up from petting their cat. I literally felt myself falling backwards as Michael caught me from behind. I laughed it off and thought I was just sleepy.
I called my sister the next day and told her I didn’t know if I could do this, that chemo was scary and much harder than I thought it would be. She told me I “just had to do it,” that I didn’t have a choice, and that it was going to save my life. My friend Alex, who is a doctor, called to check up on me and gave some great advice. He told me I was going to have to find something to occupy my mind during chemo.
Trying to concentrate enough to read a book or write something was out of the question. I tried to meditate using some guided meditations I had downloaded onto my computer, which helped some. The thing that really got me through this tough week: watching all five seasons of Breaking Bad. Walter White and Jesse Pinkman might be two bad dudes, but they saved my sanity during this time.
I slept off and on all week, which was a blessing. I felt nauseous, lightheaded, and so tired I could barely walk from the bed to the bathroom without stopping halfway. I told my husband I understood why some people opted out and refused to do chemo, especially if they’d already been through it before.
The extreme nausea lasted until Tuesday, and Wednesday I could eat and drink a little more. The nurse had told me I was going to feel like a truck hit me, and she was right.
I still had one more treatment in this first cycle, another IP of Taxol, on Thursday, the very next day. Wednesday night, however, I mustered up the energy to meet my running group at Alex’s place for pizza afterwards.
Seeing all my friends, even if I couldn’t run, was the best medicine for me. And I had a great excuse for getting out of a hot, sweaty, Texas summer run.