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Ready to Head Home

I had my final post-scan today, and we got our hotel room swept with the geiger counter. Everything is a go for us to return home tomorrow. Kathy and I are both anxious to get on that plane and get back to Gilroy.

The therapy on Wednesday went pretty well. I had the expected pain, flushing and overall discomfort with the amino acid drip. The radiation infusion went off without a hitch. It only took three sticks to get two IVs started, which is a great batting average with my arms.

Yesterday I felt better than I did immediately following my first two treatments. Today, not so much. I’m feeling queasy, tired, weak, and dealing with lots of flushing. The supposition is that all of this is brought on by the cancer cells getting fried and thereby releasing more of the hormones and other junk that make me feel lousy. I know I will start to feel better in a couple weeks, but for now this is miserable.

I’m three quarters of the way done with PRRT. There’s no question that all of this is more tolerable knowing that it’s having a positive impact. As I’ve stated before, however, I really look forward to getting that last treatment behind me late next month so I can really begin to recover without getting knocked back down.

I’ll be sure to post again sometime next week when I’m feeling a little better. Take care.

Just Hanging Out in Houston

The PRRT infusion went according to plan yesterday. It made me feel sick and tired, but a little less so than the first time. The worst part is the amino acid IV. For whatever reason it really aggravates my hands and arms where the IV is and they ache horribly the whole time. Today is a little better.

I had a follow-up scan this morning, and will have another tomorrow morning. During that visit tomorrow the doctor will meet with me to discuss the results of all of these scans. I’m really looking forward to getting some definitive information about the effectiveness of this therapy.

For now I’m just hanging out at the hotel, trying to get some rest. I talked with two of the other PRRT patients this morning at the clinic. We’re all staying at the same hotel. It’s great to see and hear how others are doing, and to feed off each other’s enthusiasm about this process. I’ll post more tomorrow after meeting with the doctor.

PRRT Today

Yesterday Kathy and I took advantage of our last day with nothing scheduled and headed down to the Kemah Boardwalk. That’s a picture of Kathy looking out toward Galveston Bay at the endless line of huge container ships sailing past. We enjoyed a great seafood lunch at Landry’s. Then we went further south to Galveston. I’m standing on the beach there with the Gulf of Mexico behind me. We didn’t realize how many cool historical homes and buildings there were in Galveston. It was a fun and relaxing day.

Finally this morning, after all of the scans, tests, and preparation, I started my first round of PRRT. There’s a picture of my recliner where everything was administered and a look at my view out the window. They started the amino acid drip first, which is administered to protect my kidneys. That caused an immediate flushing episode that was pretty uncomfortable, and caused intermittent flushing over the next four hours. 30 minutes later they started the PRRT drip, which only lasted 30 minutes. That was completely uneventful and had no noticeable side effects. When the PRRT was done, they did a scan.

Every hour or so I got a dose of anti-nausea meds because the amino acids were also making me queasy. That’s fairly common. After a couple more hours I had another scan, and the tech said she could see that the uptake of lutetium into my tumors was good. So the drug has been delivered and now we need to hope and pray those little radioactive isotopes get in there and toast my cancer cells.

We’re back at the hotel now and I’m feeling relieved, fatigued, and a little uncomfortable all over. I’m really happy that Kathy is here to help take care of me. Things are a little crazy because we have to stay in separate beds, use separate bathrooms, not come near each other and she can’t come into contact with anything that I’ve worn or handled. Friday they’ll send a tech to the hotel room to scan everything for radiation. Anything that’s “hot” will have to be bagged up, packed away, taken home with us and left to “cool off” for a prescribed period of time. Fun.

Tomorrow and Friday I’m confined to the room since I can’t be around anyone else, but I do go in for a follow-up scan each morning. These scans won’t measure the success of the therapy per se, just the radiation uptake and to make sure that my kidneys are eliminating the excess radiation. We’ll only know how successful this has been over time and after additional treatments.

Well, if I wasn’t tired before, I really am now after writing this. Thanks for reading and take care.