“Welcome to Air Infusion Flight #2. Our scheduled departure today is 8:30 a.m. from the Queen’s Cancer Clinic in room 412 of the Kuakina Medical Plaza. If you’ll just take your seat, there’s no need to fasten your seat belt. Just make yourself comfortable. We should reach our destination in only 4-1/2 hours, an hour less than on your first trip because there’s no stop today for immunotherapy.”
My first session of chemotherapy and immunotherapy on June 29 was estimated to last 5-1/2 hours. That sounded like a very long time to sit in a chair finding ways to pass the time until I realized it was about the same length of time it takes to fly from Honolulu to San Francisco. That’s a flight Meda and I took a number of times since the beginning of March while commuting to the University of California San Francisco Cancer Center for diagnosis and initial treatment. There’s a rhythm to a flight like that and, if you can get your mind into it, the time passes quickly.
Framing of my second chemotherapy session this morning as just another flight from here to there avoids having to dwell on that pesky cancer that necessitates this excursion.
I’m carrying a small travel bag with me this morning. It contains a fully-charged iPad with keyboard case, a Kindle e-reader, iPhone, battery and cable in case a device needs recharging, a couple of snacks, a medium-weight sweatshirt and a pair of nice fuzzy socks for warmth, and a travel pillow in case I want to lean back and nap. I’m also carrying my health insurance cards and driver’s license, although I probably won’t need them this morning.
I’m wearing a mask as I make my way to the treatment area, although I’ll probably take it off after that. I’m dressed for the occasion. Long khaki pants, slippers (so that it’s easy to put on those fuzzy socks), and a button-down aloha shirt so that it’s easy for Nurse Patti to reach the IV port implanted high on the right side of my chest. Although the description of its insertion was daunting, it’s a little gizmo that makes the repeated IV treatments tolerable for those who, like myself, have veins that shy away from approaching needles.
The IV feed started at 8:30, and I should be out of here shortly before 1 p.m.



