I finished the second round of chemotherapy sessions on Friday, and once again, nothing bad happened that I could recognize.  The only side effect that I noticed was constipation, but I got moving again last night, so that was just a minor annoyance.

There was one side effect of my first round of treatments that had no symptom that I was aware of:  a blood test before the second round showed that I had a really low white blood cell count giving me a high risk of infection.  This time, after the last drip on Friday, the nurse taped a small box on my stomach that, I gather, gave me a trickle of some drug that would stimulate my bone marrow.  I was told to leave it on for a bit over 24 hours and then just take it off and throw it away in the regular trash.  Again, just a minor annoyance at worst; and most of the time, I didn’t even need to pay any attention to it.

They found a really good vein on Thursday and so were able to leave the IV in overnight; but I don’t think I’ll ask them to do that again:  given the really small needles they use these days, and the high skill level of all the nurses that I’ve had, getting stuck one more time is better than not being able to take a proper shower later and worrying about messing up the IV while I was sleeping.

I’ve been tremendously fortunate so far.  I’m just n=1, of course, so my experience isn’t significant; but so far this hasn’t been bad at all.  Indeed, once I found out that I could bring my computer and WiFi hotspot with me, there wasn’t even any boredom. 🙂

My next round of treatments will be Wednesday through Friday starting on the 25^th; and the doctor said that it would be OK for me to get my next COVID booster about a week before that.

On the first of November, I’ll begin my trip to Kailua-Kona, Hawaiʻi for some meetings; and I’ll get my final round of treatments probably a couple of weeks after I get home on the 15^th.

One of the possible side effects of my chemotherapy drugs is risk of infection, I had a blood test today in preparation for my second round of chemo on Wednesday which found a very low white blood cell count, and it’s not hard to connect the two in my mind.

The nurse called me on the phone and seemed concerned about that, to the point of moving the next chemo session back a week, and ordering another lab test before the first treatment.  We’ll see how it goes.  I don’t currently have any cold or flu-like symptoms; but I might need to take extra precautions against being around other folks who are sick just in case.

I’m hoping that it’s just a mistake at the lab.  (If I were a perfect person myself, I wouldn’t be able to imagine that; but…uh…)

Somebody posted a comment that wound up in my spam folder asking about an RSS feed, but I haven’t checked the spam in a couple of weeks because of a variety of distractions.  I approved the comment, but now I can’t find it.  In any event, what I’d respond is that I’m largly clueless about RSS, but PZ could probably give a good answer.

I promised in my last post to mention some open-source code that I’ve been working on, but I’ve been distracted.

If you’re interested in what it takes to host a meeting at a hotel and convention center, read on.

The way it usually works (YMMV) is that you contact a sales rep. for the hotel and say when the meeting will be, how many folks will likely attend, and what you’ll need for meeting rooms.  In our case, for example, the meeting will last five and a half days.  Monday morning and Saturday morning will be plenary sessions*, so we’ll need a room for 100+ persons for that; but the rest of the week we’ll break into subgroups where the real work gets done, and so we’ll need a bunch of breakout rooms.

The sales rep. responds with a description of meeting rooms that will be available for the dates of your meeting, the number of guestrooms that will be held for your group, and a group rate for the guestrooms.  In our case, we’ll have 100 guestrooms held for Sunday through Friday nights and 50 for Saturday night; and I’ll be responsible for 80% of that.  (If fewer than 520 room-nights actually get booked, I’ll have to pay for some myself.)

For the meeting rooms, the usual arrangement is that, if you meet some minimum amount for food and beverage service, you get the meeting rooms for no additional charge.  I won’t have any problem meeting the minimum because the guestroom rate doesn’t include breakfast, so I’ll provide a breakfast buffet for six days along with customary mid-morning and mid-afternoon refreshments for five days.  Any A/V equipment you need for the meetings will be extra.

I still have some details to work out.  After my next round of chemo treatments next week, I’ll have a meeting with the hotel’s sale rep. on Tuesday, the 3^rd, where I’ll be shown the meeting room area and, I hope, get a few more questions answered.  The following week, I expect to actually sign the contract; then I’ll start working on the food and beverage requirements and the A/V requirements for the meeting rooms.

There’s a fellow in Germany who’s our logistics guru, so I’ll mostly defer to him re the A/V stuff.  We already have our own LCD projectors, audio mixers for the three larger rooms, and pretty much everything we need to allow folks to attend remotely via Zoom; but there are still things that we’ll need from the hotel (projection screens, microphones, WiFi for about 100 in-person attendees, stuff like that).  If, as in our case, everybody will have a laptop computer, or at least a tablet, you’ll need lots of power strips for which the hotel will charge an absurd amount.  It’s often cheaper to just buy your own power strips locally and then donate them to some educational or other non-profit institution when you’re done with them.

We also still need to decide how seating in the rooms will be arranged.  The rooms that the hotel had available for the week of the meeting all have load-bearing columns here and there (it’s an old, historic building…a good excuse) which pretty much eliminates the U-shape setup.  We’ll probably go with the classroom setup (rows of long tables facing the front of the room), although one or two of the smaller rooms might have a boardroom arrangement.

Details, details …

---

*For some reason, we use “meeting” and “session” to mean the opposite of what they mean in Robert’s Rule of Order.

I saw the best minds of my generation destroyed by madness, starving hysterical naked, dragging themselves [from room to room] at dawn looking for an [FtB] fix.

(apologies to Allen Ginsberg)

OK, it’s old news by now; but I didn’t find that Freethought Blogs was back up until I returned from a doctor’s appointment this afternoon, by which time this old fart needed to take a nap.

But I’ve finally gotten caught up on my FtB reading, so now I’m no longer depressed. 😎

I have a post in mind about some easy coding that I was doing to pass the time.  Maybe I’ll get to that after today’s TV news.

Just a quick test to see if I can capture a screenshot and play with it using IrfanView (which I’ve been miscalling InfanView for some reason).

Yeah, that works, and in the obvious way:   PrtSc, open IrfanView, create a new image, Ctrl-V, Resize/Resample, Save As a JPEG…no sweat.

There’s method to my madness:  on my train trip in November, I can do an occasional screenshot of my GPS display so that you too can see where I am. 😎

(I hope my newbie experiments aren’t boring y’all too badly.)

Here I sit in the Cancer Infusion Center writing this post.  I’m really glad I can bring my laptop with me to mitigate the boredom.

I’m finishing my first round of three treatments on consecutive days; and then I’ll have a couple of pills to take at home tomorrow after breakfast.

The first day, Wednesday, started with drawing some blood in the lab.  The young woman in the lab was really good at her job, and I didn’t even feel the needle going in.  I have no end of respect for real expertise.

Each first treatment in a session, I was told, would be giving me two drugs, the first taking about half an hour to drip, and the second about an hour; but they gave me more than that.  After inserting the IV (in an awkward spot on the back of my hand because the nurse couldn’t find a better vein), there was some flushing of the IV with saline solution, then rather a lot of some milky solution administered with a syringe that took maybe about five minutes.  Then more flushing of the IV, the two drugs that I was told about, and more flushing.

I wound up being stuck there in the hospital for about four hours with basically nothing to do, mostly waiting for the lab results to come back before they could start on the real business.  I hadn’t had any lunch that day in the hope of mitigating the nausea that’s sometimes a side effect of chemo; but I learned too late that it doesn’t show up until at least the day following, so I needn’t have skipped it.  I stopped by a Waffle House on the way home to have a big second breakfast for supper and I wasn’t able to watch the Cardinals’ game until the top of the third.

<aside>
I don’t watch enough TV for cable to make sense, so I watch the games on mlb.com’s Gameday feature and listen on the radio.  (I confess to watching Baseball Night in America on Fox because of their monopoly, but I stay away from anything Murdoch otherwise.)
</aside>

Yesterday was quicker.  I had been told that I’d get just the one drug that takes about an hour to drip (I get that one on each of the three days); but what with administrivia, inserting the IV, all the flushing, and yet another drug that I hadn’t been told about, I was there for a couple of hours.  Fortunately, I had thought to ask whether it would be OK to bring my computer with me so that I’d have something to do.  They said that that would be just fine, so I was able to spend the time writing yesterday’s post.

Today should be a repeat of yesterday, except that the nurse had found a really good vein in a good position and could tape up the IV really well after the treatments, so I was able to keep the IV in overnight, and I didn’t need to get stuck again today.  Also, the first extra drug only took about five or so minutes and was administered by syringe, so I’ll have only about one hour of dripping which started at 15:15.  I can hope to be out of here by 16:30, give or take.

I probably won’t have anything more to say about this first round unless something bad happens.  So far, I’ve had none of the usual side effects of chemo, not even a wee bit of nausea or diarrhea, and I currently have no reason to expect it to start.  (I am having frequent hiccups that started around quarter to four this morning.  That’s not listed as a side effect in the blurbs I was given about the drugs I’m getting; but I found a paper about hiccups on (IIRC) nih.gov (I can’t remember the URL and wouldn’t be competent to critique it in any event) which mentions in a table of side effects that hiccups is a possible result of taking of chemo drugs, but it’s probably not a problem unless it continues for several days.  I’m not having that side effect as I write this.)

I’ll have three more rounds of three treatments on consecutive days, probably Wednesdays through Fridays.  I have an appointment with the chemo doctor next Wednesday where we’ll set up the schedules for the final three rounds; and I’m going to express a really strong preference to begin earlier in the day so that I can get home at a reasonable hour.  It’s already known that my trip to Hawaiʻi will interrupt the sequence such that I’ll have two or three extra weeks after the penultimate round.  The doctor has said that he’s not particularly worried about that, but he’ll want more lab tests after I get back just to make sure that everything is still in order.

So far, I’ve been tremendously fortunate.  The cancer was caught in an early stage before it had metastasized to the lymph nodes (which I’m told is unusual for small cell cancer), so there was no big deal about my refusing major thoracic surgery (which I would have refused at my age in any event), and I’ve had no symptoms that I’m aware of (aside from the hiccups that I mentioned above) from any treatment or from the cancer itself.  We’ll see whether that continues…

The Reason

This old fart needed to get with the program and buy a digital camera; so I broke down and got a pretty good one for use during my trip to Hawaiʻi in November.  That will include a round trip on Amtrak’s California Zephyr through the Sierra Nevada and the Rockies, both in daylight, the latter including a ride along the southern bank of the Colorado River through Glenwood Canyon.  On the return trip, I also hope to catch the lights of Denver way down below after exiting the Moffat Tunnel a bit after dark.

Some folks might also find interesting the mostly open-air KOA airport and the quick rise from sea level in Kailua-Kona up the mountains of the Big Island.

---

The Sale

On my way to my chemotherapy appointment today, I stopped by a camera store in St. Louis County, Schillers Camera, that’s not far out of the way.  It didn’t get off to a really good start, though:

Me:  Would it be possible to find a digital camera on which I could use some screw-on lenses from my 50-year-old Pentax 35mm SLR?

Sales clerk:  LOL!

Actually, he was very polite and understanding; but the clear answer was “not easily and probably not worth it”; so in addition to the regular lens, I’ll probably want a shorter lens and a fisheye for taking pictures of my bedroom on the train, and a moderately long zoom for scenes outside the train.  Another requirement is the ability to copy the images directly to my laptop without going through anybody’s “cloud”.

The camera is a Canon EOS Rebel T7.  I opted for the “Premium Kit” which came with two lenses:  an 18-55mm zoom, which is supposed to be wide angle to normal, and a 75-300mm zoom, that should be good for shots of the train from outside and views of the mountains in the distance, along with some niceties like a camera bag and a battery charger.  I also bought an 8-16mm fisheye zoom just in case I need a super-wide angle for pictures of my Zephyr room from the inside.  Are all lenses zooms these days?

---

The Test

So here’s a trial run just to make sure I remember how to take pictures. 😎

I’m also learning how to copy the images to my laptop.  With one exception, that was really easy…just pull the SIM card out of the camera and stick it in an adaptor that plugs into a USB port on the laptop.  On Windows, it magically comes up as drive D:.  I haven’t tried to mount it on my Linux partition yet.  (Friday, 08:00:  just plug the SIM card and its adaptor into a USB port and it magically shows up as a mount point on Ubuntu Linux.)

The problem was that I couldn’t get the SIM card out with my fingers.  Fortunately, the Infusion Center’s lab had a small hemostat that they graciously allowed me to use for the purpose.  I have a really small hemostat at home that will now become a regular part of my camera equipment. 😎

The entrance to the Cancer Infusion Center is next to the emergency entrance;

but I don’t normally use that.

[trying out the fisheye] I park in the main garage (on the left), not far from the main entrance (on the right), so that I can leave my car out of the sun or rain.

From there, I have just a two or three minute walk, all under cover, to where I’m supposed to check in.

When they get around to me for treatment, I’m supposed to sit in what is thought to be a comfy chair while I get my drugs;

but the nurse said that it would be OK for me to sit in a regular chair to write this post; and she graciously provided me with one of those bedside tables that they have in hospitals.

(The boxy thing that connects by a short cable to a USB plug is the SIM card adaptor.
The black box with a button on the viewer’s left is my Verizon WiFi hotspot.)

I hope to have more interesting photos to show you in the future, at least by the time of my November trip.