I forgot to post from last week’s treatment… so I’ll do it tonight before tomorrow’s treatment. My friend, Christina Dawson, came with me. She was so helpful at the beginning of this diagnosis- helping me navigate this foreign world and connecting me with resources I have used over the last few months. It was nice to spend time with her as we’re nearing the end of chemo. I have 3 more treatments left now. I can do this… I can do 3 more!
The most notable improvement has been with my mouth sores. They are getting better and I am able to enjoy eating some foods. Mostly bland foods, but at least I can eat. My stomach is still getting used to knowing what to do with solids, but this will all improve over time.
My body is still very weak because of my weight loss and fatigue. I look forward to feeling well enough to start working out again and building some muscle. I’m not used to feeling so weak and tired for so long. The other side effects- neuropathy and bone pain continue to be tolerable.
One other difference- if you look very closely in just the right light you can see hair growing back on my head. It’s so light blonde that you can barely tell it’s there. I will continue to wash with shampoo and conditioner… can’t let a few hairs get greasy. Go Cavs and Go Pens! This is an exciting time of year… for a lot of things.
Addendum: not 10 minutes after I wrote that, I was complaining to Rob about how sore my fingernails are and whining that I don’t want to go to treatment tomorrow. I fluctuate from positive to negative just like that. Or maybe I’m always feeling some of both. Hard to describe, but it is what it is.