Today was my first chemo treatment. I have been very calm all week about this. I was a little scared of what it would be like but I was not in a panic. I actually had a fairly good night sleep on Wednesday night and woke up in plenty of time to get ready and have a little breakfast.
Kevin took me this morning. Faith spent the night at a friend's house and we had to drop John Derrick off at his friend's house. We got to the doctor's office five minutes late but we had to wait of course. I had to be weighed and have my blood pressure checked and a finger prick. I then met with Dr. Raefsky and he did a quick check and explained what was going to happen today. He told me that the bone scan and CT scan came back clean. They did see a tiny spot on my liver but he told me that it is probably a cyst and that they were quit common. He was not too worried about the spot and I would have another CT scan in about 6 months. After he left, a nurse came in to explain the medicines and the side effects.
I went to the treatment room after that. The treatment room is a large room filled with "recliners" I picked a recliner and waited. I had decided to have the genetic testing done to see if I carry the gene for breast cancer. The nurse took my blood for that first. Then I was hooked up to the IV. All of this was done using the port that was put in a couple of weeks ago. They first put in some anti-nausea medicine in first and then the chemo drugs. The first chemo drug the nurse nicknamed "the red devil" because it is red and pretty powerful. It could not be put in through the pump. She had to manually put it in me using a large syring. The second chemo drug was put in using the pump.
I was given plenty of medication for the nausea so hopefully I won't be too sick. I will experience fatigue and my hair will come out. The hair loss probably won't start happening for a few weeks. My white blood count will go down at times and I will have to be careful not to be around sick people. Tomorrow I have to go back and get a shot that will help my bone marrow to build itself back up. I also go back August 3rd to check my white blood count.
As I said, it was easier then I thought today. I met another lady who was getting her last chemo treatment. As we were talking, I found out that she teaches at Castle Heights Upper Elementary which is the 5th & 6th grades of the Lebanon Special School District (LSSD). Faith goes to Coles Ferry Elementary which is also part of LSSD. She had a real good attitude and looked great. We talked that last part of my treatment which made the time go by really quick. I was out of there by 1:00 and Kevin and I went out for lunch and then did a little shopping. We picked of John Derrick and came home and now I am sitting here typing this.
I am started to get a little tired right now. It is 5:30 and I think I will get up and put on my PJ's and sit here on the couch. Since Kevin and I had a late lunch, we are not too hungry. He left to go pick up a pizza for the kids to eat. Faith is back from her friend's house and she is tired a little sunburnt because she got to go swimming today. John Derrick is tired from playing so hopefully they will both go to bed without a fight.
Think you for all your prayers. I had such a peace about today because I knew prayers were being answered. But, I have one chemo treatment done and just 3 more to go!!