The Mister was in good spirits and felt good. So I ventured out on a little road trip for the day. I roamed small villages stopping in quaint shops and talking to the locals. It was a great reset day.
There are places in this country where hate doesn’t exist and one village is proud to let folks know. 💜
He’s past the critical 72 hour threshold and still without major side effects this round. He says some hours it feels as if he’s climbed a mountain with muscle tightness t but it doesn’t linger. He naps off and on but honestly, if this is the worst thing he has to contend with we take as a win.
A period of waiting for the 22nd of the month when the 3rd and last infusion takes place.
Onward! 💜
Five days out from his second infusion and he woke with nausea and very achy joints and muscles. I gave him one of the nausea pills the doc prescribed for it. First time taking it. He had toast and applesauce, sipped on lemon water. Feel asleep twice more in his chair since waking up.
It’s been seven hours since he took the pill and he’s now feeling so much better. Said he was hungry and he’s eating a BLT lol. No more nausea 💜😀
The Mister has done fairly well 10 days out from his second infusion. Symptoms continue on the mild side w/one new one. A mouth sore developed but has been kept at bay w/the recommended rinse. Otherwise, fatigue, muscle/joint pain seem most prevalent but manageable.
Next week a follow up w/his heart doctor to monitor the abdominal aortic aneurysm is scheduled. He'll be brought up to date on his cancer & his heart will be monitored for as well. So much to watch for while undergoing chemo.
Today the Mister had a follow up w/his heart doctor. The EKG indicated a different blood flow pattern than last year, likely from the chemo.
He’s ordered a nuclear stress test and Echocardiogram for Thursday and will be reporting results to the cancer team of doctors.
Results will be discussed in a follow up visit in September four weeks out.
All these doctors-important and necessary-but the Mister is so ready to be done with them.
The tests are done but boy this time the nuclear stress test made him nauseous with vomiting. It didn’t have that affect a couple years ago. But he didn’t have cancer nor was he a walking chemical plant then either.
He’s taken one of the prescribed nausea pills, has eaten a little bland toast, drank several bottles of water and is now sleeping. It should be a good sleep as he didn’t rest well last night.
One noticeable and big difference between the Mister's first chemo infusion and the second is that his breathing has become so much better, and his incessant coughing has stopped.
I still think the steroids have improved both some but at this point after the first infusion it had picked up again.
It's the little, yet big things we celebrate.
It’s the last chemotherapy for the Mister in his treatment plan to beat his cancer. It may be his roughest yet as ongoing infusions tend to do.
But he’s up for it. Attitude is good and it’s a beautiful morning out here. Let’s get this done.
And……he’s done! Last infusion and this part of his treatment plan is in the books.
Next up, second consult with the surgeon on Tuesday, PET scan to determine tumor markers then surgery to remove tumor and partial right lung.
After that, Keytruda (immunotherapy) infusions for a year for best results of cancer not coming back.
It’s a long road but by golly we’re hopeful and will remain in that lane! 💜
