Kate's visit to the thoracic surgeon last week left her impressed with both the good skills the doctor brings to the table, and the inefficiency of our medical system. One of the first things out of the surgeon's mouth was that she needed to see more scans (from a different angle), along with a pulmonary function test, to know how best to proceed with the surgery. From what Kate said it sounded like she'd decided how best to proceed before she ever walked into the room. My question is this: the scans couldn't have been done in the weeks Kate was waiting for the appointment because, ????
So now, we wait some more. The scans are scheduled for this coming Friday. (?? Happy Birthday, Kate ??) She meets with the doc a second time the following Friday.
The basics of the information haven't changed - they won't be able to begin to formulate a treatment plan until after they can get in there and see what is lighting up the scan.
In the meantime, I am encouraged by words I hear them using, still.
Operable. Treatable.
These are good words. Words of hope. Words helping me to keep a sense of balance, of center.
Already, as this storm comes in to land, I am held in the arms of love. It's the same sense I felt in 2012, when I found my lump. In 2015, when Kate found her lump. In 2017, when Libby found her lump. (You women out there reading this, you ARE checking for lumps regularly, yes???)
This road is a tough one, no question. But I do not walk with her on my own, and that makes it oh-so-much easier. As I've spread the unwelcome news, I've heard SO many times, "I'm pretty sure there's nothing I can do to help, but if there is anything I can do, please ask."
I've begun to plan my trip to be with Kate for the surgery, and I have heard 'yes' from every person I've asked for help. There is someone to walk the dog, to pick up the mail. The lawn will get mowed, the plants tended. And, there is someone to take over Fairy Wren duty while I am gone - a child's imagination is important ground to keep watered!
Take one more step...