Before I went to MDA the second time, I got very sick with fever and we didn't know where it came from. I just know I didn't feel well at all.
Dr. Yao said my liver function was improving, so he thinks the chemo is working. I really hope so. I feel so much better this time after chemo than I did the first time. I have so much more energy and I am not near as weak. My chemo is still 8 hours long for three days which is long, but I sleep most of the time.
Next time I go, we take blood work, then we take CT scans of my abdomen. My prayers are that the tumors are shrinking. After I talk to Dr. Yao, I take my treatments. I asked him how long my treatments would be and he said we would evaluate every two months. He is all business!!!! As his PA's say, he is all cancer doctor.
We are staying at the Rotary HOuse which has a skyway and is connected to everywhere I need to go. Even when I shut a building down, I just go to my room, and if the gold carts are running, then Travis pushes me in a wheel chair.
I don't know if I told everyone, but I did try to save my hair, but the girl who cuts it tried to save it short, but it kept coming out. It is as short as you can get. When I was in Houston, I bought some cute little hats that color coordinate with my clothes. Sometimes, I'm self conscience, but this is real life and I can't worry about everything. A friend gave me a small cross before I went to MDA and I'm all about prayer. It is called a Clinging Cross and it fits into your hand. It is the coolest thing. I know I don't have to use it to pray, but it seems to make me stronger.
I am very fortunate that both of my kids, Jennifer and Travis went to MDA with me this time. I didn't want Gary to miss work. My kids are super supportive and are very positive. Right now the plan is to go to MDA every three weeks to get my chemo.
I will refer people back to my blog on FB. Thanks for reading.
Susan Hall