So today I have been doing some research on what to expect for Chris in the third round of chemo and beyond. We have been talking in the abstract about our summer plans “after chemo”, uncertain how long it will take for him to feel like he is on the mend. So I figured seeing what other people may have written about their personal experiences would reveal.
In that search, I found this blog: http://austinelling.us/content/testicular-cancer-beginning
In it, blogger Austin Elling gives a concise rundown of each stage of his testicular cancer journey, from diagnosis, through surgery, sperm banking, and each of the three rounds of chemo. It’s a pretty easy read without too much detail, but enough to get the story across. Sounds like his symptoms in general surround chemo were more intense than Chris’ have been, but it is striking how his story and his wife’s perspective (also shared in the blog) unfolded so similarly to ours. Check it out if you’re interested!
We were in the office today for Chris’ labs, weekly doctor followup, and Bleo treatment. It’s a “short day” by all standards, only taking about 90 minutes in the chair, maybe 30 minutes for the labs and doctor’s chat. Wednesdays are ridiculously busy every week we have been there, with every chair full. So luckily sitting in the hard back guest seats isn’t so bad on short days.
We had a bit of a wait in the lobby before being admitted, however, which means I got some quality PUZZLE TIME! There is a puzzle table which resides smack in the middle of the waiting room, where you can pass the time before visits, or even during if you want. I enjoy puzzles very much, always have, but it is an extra treat when sweet little old ladies who are in for their treatments sit down next to me and we chat about this and that as we work. Continue reading
Shay here with a little mind-dump.
It’s funny how some events in your life can really fill your field of vision, where everything else becomes hazy and easy to forget, while the One Thing takes center stage. You allow yourself to drop the ball–you can see yourself doing it, but it’s like a slow motion scene where you watch it drop and you don’t even try to reach out and prevent it from happening.You just kind of furrow your brow at it at it and let it go.
That’s kind of how the days have been passing in the last two months since we learned Chris’ diagnosis: not slowly, but…groggily? and without much of my own motivation moving things forward. Continue reading
Well, it’s been a lousy day so far, but it’s getting better. Continue reading
So, I’ve been a bit remiss in my blogging. Apologies to everyone (anyone?) who may be reading this blog and missed me! 🙂 This really is my first time trying to maintain any sort of blog, or personal public website – so bear with me. Continue reading
It’s been a little while since we posted anything. Not because nothing has been happening, but because a lot has been happening and it’s been hard to find time and motivation to post. But we have been thinking about all our friends and family reading this blog and wanted to post some pics and talk a bit about what all has been going on in Casa del Moore.