My mom crafted these wise men somewhere way, way back in the 1960s. They’ve held up remarkably well.

My mom crafted these wise men somewhere way, way back in the 1960s. They’ve held up remarkably well.

Most poetry leaves me confused, but I get this one.
It says what I’ve been feeling:
“I want you to believe that the Universe is a vast, random, uncaring place, in which our species, our world, has absolutely no significance. And I want you to believe that the only response is to make our own beauty and meaning, and to share it while we can.”
Growing up, I was taught that it was important for me to use my talents and smarts to do something big to make the world a better place. I have realized several things over the years regarding this goal:
More and more, I think that the whole idea of just being kind to others, of actually practicing the Golden Rule, has more of a chance to better the world than most anything else. Which leads me to flower gifting.
I have been making paper flowers since 2017. I never made them with the goal of selling them, I just enjoyed the process. This means that over the years, I have given many flowers away and never more so than in the last few months.
Since August, my physical therapist’s office got several bouquets of tulips. One of the receptionists there took a bouquet of various wildflowers with her when she moved to Texas; the other receptionist got a bouquet of daisies and roses. My physical therapist got a pink rose for her birthday last month. My landscaper took several roses home to his wife. My home-health nurse admired my water lilies and now has one sitting on his desk at work.
If you are around me long enough, I will probably ask you what your favorite flower is and try to foist one off on you, for example:
When I look at all the flowers I have made and given away over the years (which you can see if you look under the Paper Flowers heading here on my blog), I like to think that I am, after all, doing my little bit to brighten up the world.

(Many of the flowers I make are thanks to the designs and techniques found at https://liagriffith.com/craft/all-paper-flowers/. If you’re interested in making flowers or many other things, her site is hard to beat.)
After a few people this year told me how much they like their bidet, I went out and got one. Now I wonder why the hell these things aren’t standard in every household. They’re freaking awesome! And they save a tremendous amount of toilet paper, so better for the environment. Win, win!
(And, no, I don’t feel bad about the amount of water it uses even though I live in the desert because Henderson recycles 99+% of the water that goes into the sewer system.)
According to the internet https://bestmoderntoilet.com/which-countries-use-bidets-the-most/:
I wasn’t sure whether I’d use all the options on it but have to admit that I turned on the water-warming feature almost right away. And now that cool weather has finally arrived, I have turned on the seat-warming feature. A warm seat in the middle of the night is a surprisingly wonderful luxury.
Getting one is not a huge expense, either. Mine is the Brondell LE99 Bidet Toilet Seat which is around $300. I did have my handyman put a GFI outlet in by the toilet, but that’s not a necessity as long as there is power somewhere nearby.
In short, if you don’t have a bidet, get one! I can’t imagine you’ll regret it.
I was only in the hospital for 2-1/2 days with my stroke, mostly waiting for tests to be scheduled. I was totally ambulatory the whole time and did not require much in the way of attention. I talked to the nursing staff at change of shift, during blood draws, etc., but didn’t interact much with anyone other than that. Yet 2 people came up to me to thank me for being so nice.
The first was the man delivering meals. Now I don’t think I did much other than thank him for delivering the tray and taking it away. And even at that, I wasn’t there for several of the meals, so I only saw him a few times. And yet he made a point of thanking me for being “so nice” unlike many other people.
The nurse on the evening shift also thanked me for being so good to work with. Now in her case, I think my “niceness” was just in comparison to the woman next door who, admittedly, sounded like a handful. Still, being called “nice” twice in one day seemed odd.
Then the next day when the home health nurse arrived, I was told the same thing. Again, I have no idea just what behavior of mine they found so remarkable.
It seems a sad commentary on society when merely being polite counts as being nice!
Since my little stroke, I have had all sorts of thoughts about life and death and what kind of life I hope I am living and other such stuff. I have had lots of things I want to write about, so much so that I’ve been a bit overwhelmed trying to tie them all together.
The answer, of course, is to give up trying to make one cohesive essay and write down lots of little ones as thoughts come up. That’s what I am going to try to do.
So first: having a stroke has thrown me more than I think a heart attack would have. I’ve always sort of assumed I might be done in by a heart attack someday. In fact, I’ve always said that my preferred method of dying would be to have a big enough attack that I just didn’t wake up some morning.
(Which leads to thoughts of “Who would know if that happened?” “What about my dog?” “Would the cleaning people come in days later to a real mess?” Ah, the problems of living alone.)
But I had never considered a stroke. The idea of being alive but unable to do anything is absolutely frightening to me. I think I would be more than ready to do the hard work if recovery was possible, but what if it wasn’t? The idea of being shuffled off to some nether world that was in the twilight zone between living and dying is anathema to me. Which is why I have given very detailed instructions as to what I want to the person who has my health power of attorney.
Which is not to say I’m planning on anything happening anytime soon. In fact, today’s good news is that the follow-up CT scan I had on Monday shows that all is stable.
Meantime, I’m spending at least an hour a day reading aloud and/or singing. I’m a little closer to being able to hold a note!
Had someone who saw my tulips at the physical therapy office ask me to make her a bouquet of 13 flowers in some specific colors: 4 dark pink, 2 light pink, 1 gold, 2 dark orange, 1 light orange, 1 purple, and 2 yellow.
I ended up making 2 sets; both sets started with white crepe paper. I colored one with inks and the other with Pan Pastels. The inked ones on the left seem a little more delicate to me, but I like them both. She liked them too; she bought all 26 of them!

10 days post stroke and I am doing quite well. My speech is basically back to normal, just need to be careful not to talk too fast. I have discovered one other side effect, though: I can’t hold a note at all.
On the morning of the stroke one of the things that clued me in to the problem was that I tried to sing the “Do, Re, Me” song to my dog and could not hit the notes. I still can’t. I’ve gone from having what I call a “decent community choir” type voice to one that grates on my ears.
A big solution to improving my speech was reading aloud; I have been doing that for an hour or so a day. Going to see if singing along to some songs will improve my voice in the same way. Trisha Yearwood songs are almost entirely in my range (or at least they used to be!) so I’ll be singing along to those while I sit in front of the computer.
Monday morning after breakfast, I was talking to my dog and realized I was slurring my words. Got to the emergency room and they started tests. Turns out I had a very small stroke. The only thing affected seems to be my speech; I have to speak a bit slowly and must be careful to enunciate clearly.
Got home yesterday afternoon. Spending this morning trying to set up all the follow-up visits with neurologist, cardiologist, primary care doctor, etc.
I was, of course, supposed to be going on a 33-day cruise starting next Wednesday. Another task for today will be cancelling that and talking to the insurance company about getting some money back.
I have a lot of thoughts about this whole situation, but I find I’m not ready to put them down yet. Mostly just thankful for all the people who have offered to help out.
A year ago this month, my mom celebrated her 99th birthday. During the week of her birthday, we went out one morning for her favorite chocolate-chip waffle and on another day, a chocolate milkshake. We had cupcakes on the day itself with her friends at her assisted-living home.
On that day, I told mom that her doctor was already making plans to throw her a big party for her 100th birthday. Mom looked at me, shook her head, and said “No, I’m not going be here for that.” Four days later, I got a call to say she had fallen and had been taken to the hospital.
Turns out her right femur had broken. Her left one had broken back in 2019 and she had surgery and recovered well. But now, at her age and with some heart irregularities, fixing the leg was just not possible. She was sent back to assisted living to spend the rest of her days lying in bed, unable to move, in constant pain, and perfectly conscious of all of these facts.
As you can imagine, she was not happy with that state of affairs and wished she could do something about it.
The Nevada legislature earlier that year had passed SB239, which “would have allowed terminally ill Nevadans to self-administer medication to end their own lives. The bill contained a number of steps to ensure the decision was not influenced by others, as well as legal protections for medical personnel involved in the process.”
Govenor Lombardo vetoed that bill, stating: “SB239 allows for physician assisted suicide in the State of Nevada. End of life decisions are never easy. Individuals and family members must often come together to face many challenges — including deciding what is the best course of medical treatment for a loved one. Fortunately, expansions in palliative care services and continued improvement in advanced pain management make the end-of-life provisions in SB239 unnecessary.“
My mom is now left with the certainty of never getting out of bed again, having to be catharized, being in incredible pain (in spite of heavy-duty pain meds) whenever they have to roll her from side to side and there is nothing, nothing, she is capable of doing about it.
My family has always been very proactive about preparing for end-of-life issues: trusts, wills, financial power of attorney, medical power of attorney, and POLST (Portable Medical Orders). Amongst other things, Mom’s POLST specified that was not to be resuscitated, not to be given a feeding tube, and was to be given palliative care.
Mom, at this point, is perfectly capable of stating that she does not want to live any longer in these circumstances. And yet there is nothing proactive that she can do and nothing that I, or anyone else, can do about the situation.
Mom’s response was to quit eating and, eventually, to quit drinking. Some 18 days after she fell, she passed away in the morning of the 31st.
It pisses me off that I wasn’t there to hold her hand, because I couldn’t be there 24/7 for the several weeks if took her body to fail. It pisses me off that I have more options for taking care of my dog than I had for taking care of my mom. It pisses me off that some politician gets to decide what is right for me and my family in situations like this.
One year later I obviously find it incomprehensible that in spite of the explicit instructions given by my mom, she had to suffer unnecessary pain for weeks.
How about letting the person and family members involved make their own decisions! My politest response to you, Govenor Lombardo and your “advances in pain management”, is to “get stuffed”.