Tired

Hi folks-
Tired is what this newest chemotherapy drug makes me. I slept through the infusion, during the car ride home, hours & hours once Steve put me back to bed, and slept most of Friday away. I sleep 14hours a day, easily. Most of you know that, I really hate sleeping my life away (I'd rather be up and about doing & living), but I'm just going to assume that my body is still healing and I need the rest; therefore still living!

I'm not doing much away from the house. I went on two outings this past week (not including the hospital), one being the movies. What fun that was to go out on a date! I felt a little self conscience about wearing oxygen out in public, but that feeling didn't last long. It sure did feel good to do something "normal".

My next chemo will be Friday, because of Christmas. This way, I get to stay awake for the holiday,which is turning out to be extra special, because Cas (the son) was able to come back and spend the holidays with us. Yipppeee!

I hope your Christmas is as blessed as our's is. Take care....