SPCU (special procedures care unit) room 12 is my room. For some reason, I always get assigned to that room. Next time I think I will bring a little plaque to put on the doorway so everyone knows.

Today, they drained 700 ml from my lungs after only 70 hours. That is a lot for such a short time! That means the fluid is producing faster and faster.

As soon as the Dr. confirmed with the ultrasound machine that I was as dry as possible, he pulled my chest tube out. I am chest tube free!

Now we need to pray that my incision will heal up at the top where the chest tube went in and that we will figure out if it’s best to put a permanent catheter or if I should keep going in and having my lung drained.

It’s hard to decide what to do.

The catheter is permanent. They put them in. They do not take them out. I would have it for the rest of my life. It was hard to hear the doctor talk about how they only do that for patients when it’s getting closer to the end of their life. They don’t plan for it to be in for years. That’s the native side of the catheter. The positive side is that I could drain it whenever I need to and would not have to go in.

The other option is to keep going in and having it drained. This involves a COVID test (12 hours to get results) or if there’s no time for me to have that, they have to treat me like I have COVID. That isn’t the end of the world, just more work for them and possible COVID exposure for me. Every time they do that procedure, there is a risk of a little air getting in like this last time, and then I would need a chest tube again…..which would then fill up quickly with liquid…lots of complications with that if I am producing as much liquid as I think I am.

We know there is a surgical option as well, but Dr. Leung does not recommend it based on what he has seen it do to other patients.

I am so thankful for the knowledgeable radiologists we are working with. The nurse we had today was wonderful as well. Her name was Alex. She was so kind and caring and gave me time and held my hand when she knew I just needed a little extra time to think before answering a question.

I’m doing okay tonight. My breathing is not fabulous. But I’m sure I’m already filling up with liquid. They did a chest x-ray before I left and everything looked good. So I’m home for now and I know what to keep an eye on.

The discussions that Tom and I are having to have are so difficult. Today we talked about where I would want to be buried and those kind of things. He just mentioned that at some point we needed to talk about it, and since we were sitting there alone in my special room 12 of the SPCU, why not just get it out of the way and do it then, right? So that’s one less discussion we now have to have. Glad that’s over.

I know that as this disease progresses my blog posts will get harder to read. If you subscribe to my blog by email please know that I will not be offended if you unsubscribe and don’t want to hear about it at 8:00 in your inbox at night. You can always go straight to the blog. Or you can always just check in occasionally and pray. The Lord knows what’s going on.

From the beginning I said I would be transparent and I don’t want to stop that now. I hope and pray that by sharing what’s going on with our family, it will somehow help someone else in the future.

As you pray for our family, please pray that we will all sleep well tonight. I am thankful I am home and can sleep in my own bed! My dad and Else just arrived up here for a 5-day visit. Please pray that our visit will be relaxing and please pray for quality time together. Will you also please pray that the chemo will do it’s job and that the cancer cells will die and that my body will stop producing so much fluid. Thanks!