The year that changed everything - part 2

 

   This is the second of two parts.  I encourage you to read both in one sitting or in relatively quick succession to get the full impact.  (If you read the first part when it was published, I encourage you to review it before read this part.)

   I didn’t realize how much happened in this time period until the last year or two. As I’ve written a few times before, I’ve been thinking a lot, for better or worse, about my life before my spinal surgery six years ago this month, and it occurs to me that an astonishing number of dramatic, meaningful events happened in the year before the surgery, not unlike the climax of a novel or, more appropriately in this case, the first or, again more appropriately here, second or third act of a drama.

   In some ways, it has been difficult to write this, as it has brought up many emotions, but I sensed it would be good to write it out, let it go, unburden myself, so to speak, so that it would no longer weigh me down.  At least not so much.    

 

   The year before my spinal surgery, which left me far more disabled, which changed everything in my life, was barely halfway over, and there were plenty more dramatic and significant events yet to come. 

   When I made it home without a van from the trip north in June, I was stuck.  Literally. I had no van.  Not only that, but we didn’t know if I’d be getting my van back or if I would be getting a new van.  And we didn’t know for a few weeks. 

   It seemed that the auto mechanic and the insurance people kept going back and forth about whether or not my van was totaled – my dad kept giving me different reports – and I was in limbo in the meantime.  Fortunately, I didn’t have much going on – no appointments and whatnot at the time – but I had to tell my attendant what to buy at the market, couldn’t escape to the beach on the weekend.  I do have vague memories of going to an event or two in L.A in an attendant’s car, taking my manual wheelchair, but I’m not certain about what and when the occasions were. My dad was also in limbo, waiting to find out if he’d be getting my van back or would have to get me a new van, not to mention how I would get either down here in Claremont.

   Finally, both to my surprise and my relief, it was determined that my van was totaled. Things were able to move forward then, once my dad received a payment from the insurance company.  Within another week or so, he located a wheelchair-accessible van – a used one – at a dealership up in Santa Rosa, and it was delivered in the next week.  (At the time, I was lead to believe that it was the only such van he could find and that it was lucky that he found it, but I have since realized that I was somewhat naïve to believe this and that it was really a matter of the price being right.)

   By the time the van showed up at my house, it was almost mid-July, and I was tremendously relieved – not only because I finally had wheels but also, and more importantly, because it meant I was able to attend the California WorldFest, a weekend music festival featuring bands from all over the world which I had attended for about five years, in Grass Valley.  Barely.  As I recall, I got the van two or three days before I had to leave. 

   On the way up, I stayed in Berkeley with my friend Leslie, who I had encountered a month earlier after 30 years, in her hard-to-get, rent-subsidized, wheelchair-accessible apartment. While there, I learned that her attendants, including Ingrid, who had been so helpful when we met in June, were provided by Easy Does It, a remarkable service available to Berkeley’s disabled residents. I was also quite taken with Leslie’s cat, Goofy, who surprised me by not bothering me at night despite my sleeping next to the cat perch.  And to my amusement, Ingrid offered us packaged cookies, calling them “crap” (I didn’t partake).

   I also stopped by my parents.  This time, my mother was up in her wheelchair and doing relatively well.  She and my father and I went and sat outside and had a nice conversation.  I don’t remember what was said, but my mom was at peace and pretty much said she would be alright and I would be alright. 

   As usual, I had a fantastic time at the festival, camping for three nights and spending the days enjoying an incredible smorgasbord of bands from all over the world on the grassy, woodsy Nevada County Fairgrounds.  I’m pretty sure Carl, my Quaker friend who is similarly disabled and who I’d met a couple years earlier, came on the last day, and we – Virsil was with me on this trip, as I recall – went to his place at the Sierra Friends Center/Woolman School, where he worked and lived, outside Nevada City that night. I don’t remember how long we stayed there, but, as usual, it was very nice, and we went home via Lake Tahoe and the back-in-time drive down Highway 395 with the usual overnight stay in Bishop.  A nifty way to break in the new van, which I was very glad to have but didn’t like as much because, for one thing,  it wasn’t as convenient for me to sleep in with its folding ramp. 

   Being back home was a chance for a breather, but not for long.  A week or two later, on a Sunday morning, someone called a left a message when I was getting up.  It was July 24. I listened to the message once I was up, and it was my dad telling me to read the e-mail he had sent.  I thought this was odd, especially as he sounded so quiet.  I read the e-mail right then.

   My mom had died.  In the e-mail, my dad wrote about how my mom had been doing okay, relatively stable and comfortable, and had taken a sudden turn for the worse.  He ended the e-mail saying my mom had always loved me very much.  David was working, and I showed him the e-mail, and he hugged me as I cried a bit. 

   I went to meeting, but I don’t remember if I said anything about what had happened. I went to a birthday party that afternoon where some of my Quaker friends were.  I don’t know if I broke the news there, but I think we talked about it.  We were out on the patio, once they realized I was outside and the house was inaccessible. 

   I remember over the next few weeks, I was very emotional.  I would just start crying. I was very thankful that I had seen my mom, calm and at peace, a few weeks earlier, and I imagined her telling my dad to hurry and get me a van so that I could come see her. 

   Also during this time, my relationship with Carl was evolving in surprising and exciting ways that made me very happy. I found out that the memorial for my mom was scheduled for mid-August, and Carl and I planned to spend time together before and after I was going to be in the Bay Area for the memorial.

   The plan was that I would go with Virsil first to see Carl at Sierra Friends Center for a couple days, then to the Bay Area for a couple days, during which I would attend the memorial, and then finally to meet with Carl at Quaker Center in Ben Lomond in the Santa Cruz redwoods, a place I cherished from going there for years for year-end retreats.  It was going to be a fun trip with some serious business in the middle.  At least, that’s how I planned it. 

   At the Friends Center, it became evident that Carl’s and my relationship was continuing to evolve – rapidly, in surprising and confusing ways.  I went to the Bay Area all the more rattled and was glad to be staying with Leslie. 

   On the morning of my mom’s memorial, I hadn’t urinated since the previous day and still couldn’t. I had had this problem before, and it became clear that I had to be catheterized – before the memorial at noon. I had been catheterized – a tube inserted into the penis – only a few times before, and it was still a very painful and relatively traumatic experience.  (After the spinal surgery, when I had to have an internal catheter all the time and it had to be changed at least once a month, the process was routine and got to the point where I barely felt it.)

   While I was nervous, to say the least, about having this procedure done and about getting to the memorial on time – not to mention still thinking about what was going on with Carl and me – Virsil and I set out on what ended up being a frantic search.  We went to two places that wouldn’t do the catheterization before we ended up at an E.R that would. Miraculously, they took me rather quickly and then did the procedure and discharged me in under an hour, as I recall.  Virsil and I were amazed that we literally pulled up to the memorial right in time and that I was in relatively good shape. 

   Actually, it was the second half of the memorial.  It was a lunch, held at a dance studio owned by my sister-in-law.  The first half had been a ceremony on a boat out on the bay, during which my mother’s ashes were scattered and which was inaccessible to me (and which I couldn’t have gone to anyway). This bothered me a bit, but the lunch was quite nice, with many relatives and friends I hadn’t seen in a long time, including one who was now a lesbian and was pleased that I too had come out.  After everyone had gotten their food, people stood and shared memories of my mom – sort of like a Quaker memorial meeting – and my sister read a piece that I had written. All in all, it turned out to be a pleasant and also emotional and, yes, traumatic day. I remember going to Telegraph Avenue to buy something – I forget what – before happily returning to Leslie’s apartment. 

   I think it was the next day when Virsil and I headed down to the San Jose train station to pick up Carl and went on to spend a few hours in Santa Cruz before going on to the Quaker Center.  Things didn’t go as planned, as Carl’s and my relationship was again quickly evolving in dramatic and difficult ways.  Even so, I made the best of being in this beautiful spot amid the redwood trees that was so familiar and so cherished, and, on the morning before Virsil and I left to return to Claremont (did we stay overnight in San Luis Obispo?), I made a point of spending some time talking to Carl.  I was very happy that we came to a resolution, as emotional and difficult as it was.           

   That Fall was relatively quiet – thank God! – although not without some significant happenings.  For one thing, I was conflicted about a local men’s group that I was involved in.  I had been quite pleased when I discovered and joined it – part of the Mankind Project – a year earlier, but it was more than the simple rap group that I was looking for. (It wasn’t really like the California Men’s Gathering, which I had been involved in for years, but I was looking for something more local, and I could get to these meetings in my chair.)  Plus, I felt pressured to attend a weekend initiation, which cost $700 ($1400 with my attendant) and which they wouldn’t say anything about.  While I was glad that there was group where men could look at their lives, express themselves authentically and recognize how they might improve themselves, I was uncomfortable with, among other things, cult-like aspects and the cost of participation. The trouble was that I wanted to stop going, but I didn’t want the guys to think I was giving up, couldn’t hack it – perhaps because I’m disabled. So, I kept going, although no longer every week, even though I was stressed and unhappy.

   In late October, at Carl’s invitation, I went to the Fall quarterly meeting, a Quaker regional gathering, in Northern California at the Sierra Friends Center.  It was a bit odd for me to be going – I usually attend the one in Southern California – but it was a way to see Carl.  The weekend turned out to be weird and kind of difficult.  It poured the whole time, making the site a big mudhole hard to navigate in a wheelchair, and, although I stayed at Carl’s house, I hardly saw him, since he was very busy with logistics for the meeting, which was part of his job at the center.  I wondered at the time if this was his way of gently setting new boundaries in our friendship.

   There was also the stressful presidential campaign, with Donald Trump (really?) all but stalking Hilary Clinton, and the surreal, stomach-churning election. After watching the exhausting election night coverage, perhaps foolishly, I was devastated by the result, leaving me in a daze for days.  This was even worse – far worse! – than when Reagan or George W. Bush won.  If anything, Carl, who was a straight-up Berner, seemed more upset than I was, barely speaking.  The on-going news about Trump’s cabinet and advisor picks – Steve Bannon! – didn’t help. 

   In late December, after Christmas, I went north again – again! – to see my family, this time with David. Once again, we stayed with Leslie, and, since we arrived during Hanukah, I took her some chocolates imprinted with dreidels, and we watched as Leslie’s attendant lit the menorah and they recited a Hebrew prayer. A highlight of the trip, and really a highlight of my life, was spending a day with Carl, who was staying at a friend’s house in Berkeley.  After having lunch at Nation’s, where, to David’s and my amazement and amusement, Carl promptly ordered another burger after finishing one, we spent some time in the all-but-abandoned China Camp park, and then I took Carl to meet my father. David and I sat in awe as Carl, who had studied computer science at Haverford College, and my dad, who had taught math at Harvey Mudd College, talk higher algebra, which neither of us understood at all.  I felt that, with this visit, with my dad liking a guy who he knew I liked, he saw and appreciated me, who I was, more than perhaps he ever had.  The day ended with Carl, David and I having dinner at Gaumenkitzel, a German restaurant I like in Berkeley, and then helping Carl get a burrito, at a tiny, surprisingly good Mexican restaurant (more like a stand) for the next day before dropping him off. 

   It was a month and a half later when, six years ago this month, in February, 2017, I got sick and ended up having life-saving emergency spinal surgery at nearly midnight on the 28^th (as I wrote about in two previous posts - October 1 and 6, 2020).

 

   In the months after the surgery, while I was in a “skilled nursing facility” – a nursing home (what happened after the surgery should be the subject of another post or two) – Carl moved back east (he would later return to California for a while). And, out of the blue, Leslie died in Aprilat age 55, a year or so younger than I was.  I was stunned and overwhelmed, to say the very least, by how much and how fast everything was changing – I cried a lot - and my dream of Carl, Leslie and I getting a nice, big house in Berkeley – ha! – and pooling our attendant funds and hiring people to be there 24/7 was just that – a dream. (I have come to realize that seeing Leslie during this year, with her increased disability, was like seeing myself after the surgery.) I also thought that it was all-too-appropriate that I fell ill one month after Donald Trump was inaugurated as president, and I was grateful that my mom wasn’t around to see both.

The year that changed everything - part 1

 

   It has now been almost six years since taking ill and needing emergency life-saving spinal surgery which left me far more disabled.  I have written about how this happened in February 2017.

   I have mentioned in the last several months that I’ve been thinking about how much my life has changed. In my last post, I wrote (actually in my latest Claremont Courier column) about how my life has changed even as or perhaps even because I incorporate certain elements from my life before the surgery.

   I’ve also wondered, as I believed I’ve also mentioned, why I’m thinking about all this perhaps more than ever all this time after the surgery.  Maybe I’m wrong, but it seems to me I would have moved on from on from such musing by now.  A friend tells me, or reminds me, that this past will always be with me. 

   In any case, I am increasingly aware that the illness and surgery were really the culmination of a year, an extraordinary year, of dramatic events, extraordinary, dramatic events.  I don’t remember if I was aware that this year was changing my life or would end up with my life changing so much. 

   The year actually started some 14 months before, in December 2015, when I went up to the Bay Area just after Christmas to see my family.  I learned just before going north that my mom, who was in her 80’s, had fallen when she was alone and tried walking without her walker and had broken her hip. This meant a good part of the visit was spent going to the nearby hospital in San Rafael to see her.  (A few years earlier, my parents had wisely moved to a senior living community with a nursing facility on the premises.  My dad didn’t really like it, not only because, ironically for its Bay Area location, most of the residents were conservatives, but he really moved there for Mom, who was quite happy with all the social opportunities.) My attendant David told me often to take it easy and stay calm and gently reminded me that things could have been much worse.  Indeed, to his great amusement, the first thing that Mom said when she saw me on my initial visit was, “Can somebody comb his hair?” As if a nurse would come running in to do it. Yep, she was still Mom.

   Except that, as my dad kept reminding me over the next months, she wasn’t. In long, almost regularly scheduled e-mails, Dad reported, or, more accurately for him, lamented and/or complained that Mom wasn’t “trying hard enough,” wasn’t keeping up with her rehab exercises, and was not getting better.  In other words, much to his frustration, Mom was going downhill. 

   I had the chance to see this for myself when it turned out that Pacific Yearly Meeting, the big, annual regional gathering of Quakers, was taking place at Walker Creek Ranch in rural Marin County, about an hour north of where my parents lived, in June instead of later in the summer as usual. But it turned out the my visit while staying in the Bay Area before heading further north for the 5-day gathering, once again with David in tow, was going to be considerably more fraught.    

   David and I had just gotten off the 1-0-1a and were just down the hill from my parents’ residence when something went wrong.  At least, that’s what it felt like at first.  I didn’t realize that we had been hit.  It was nothing like what I thought being in a car accident would be like.  There was no looking up and seeing a car coming, no screeching of tires, no shattering of glass, no airbags filling.  It was like it happened in slow motion.  I didn’t even realize we had been hit – and we were hit in the front on the passenger side, where I was sitting.

   But we had been hit.  We were in an intersection, literally at a gas station – how handy!  David and I were rattled, but he managed to pull into the station (I don’t remember if we had help with this), and when I got out, I saw that the front of the van was crumpled, smashed in.  It wasn’t pretty.  When I look back now, I’m amazed that the windshield wasn’t damaged. 

   Obviously, I was upset about this, but I was at least as upset that my dad had to be involved.  Of all the times and places for this to happen.  David called my dad, and he came right down and, surprisingly, was pretty calm and understanding. This helped, as David and I were pretty rattled, and I was in no shape to face his questioning.  While David traded information with the other driver, my dad called for his retirement community’s wheelchair-accessible bus to come down the hill and pick me up.  Sometimes, such services are especially handy!  We gathered all our stuff – hats, glasses, whatnot – out of the van, hoping but not sure if we’d see it again, and headed up the hill when the bus came. (It turned out that we ran a red light, which was a surprise to me, and, unfortunately, David later ended up having to pay a $500 fine.)

   It turned out that my mother was having a difficult time and was in the nursing facility.  As unfortunate as this was, it turned out to be for the best, because there was a lot to deal with, which we realized as Dad served up lunch.  First and foremost, how was I going to get anywhere, even back to the hotel, without a wheelchair-accessible van?  Then, should I just go home, or should I go ahead and go to the meeting? 

   Again, my dad surprised me – twice.  First, he agreed that we should try to get to the meeting, and, secondly, it turned out he and David made a good pair. They got on the phones to find a wheelchair-accessible van to rent, which turned out to be a real challenge, even in the disability-friendly bay area.  They finally found one about an hour and a half south.  So, after we finished lunch, Dad and David left me to while away the next few hours until they returned with the rental, and then David and I went back to our hotel in El Cerrito and then to dinner with my sister and her boyfriend (now husband) in Oakland. 

   Getting the rental was especially important to me, because we were giving my friend Carl, who uses a wheelchair, a ride to yearly meeting.  I was so glad we could come through for him, and picking him up at the train station (Carl is something of an expert at riding the rails – and also flying – with a wheelchair) in Martinez the next morning was all the more exciting.  An extra treat was seeing John Muir’s house in the small town, as David and I had an hour or so to kill before Carl’s train arrived.

   We arrived, intact and happy, at Walker Creek Ranch, a most cherished spot of mine in the beautiful, serene, golden rolling hills of rural Marin County, and were thrilled to be sharing a room.  But there were things that were not settled and that had to be worked out.  Little did we know what wonders this would lead to. 

   For one thing, the van had to be returned, as it was quite costly.  After getting me and Carl settled, David took the van back to San Rafael.  From there, he and my dad took the van back to the rental place, and Dad then drove David back to Walker Creek Ranch.  This all took at least four hours, during which they also had dinner and, from what I heard, developed quite a nice relationship, with my dad, retired math professor that he is, encouraging David to pursue his studies (which he has to this day).

   There was also the fact that we, including Carl, didn’t know how we were going to get back to the Bay Area, much less home (Carl lived near Grass Valley), after the meeting was over.  As I told several people, I felt, very appropriately for a religious setting, that I was truly in God’s hands.  I had to trust, to let go, to let God. I had often experienced heightened spiritual awareness at this gathering over the years but nothing like this. 

   I was thinking about this when, perhaps on the second morning of the five-day meeting, I noticed a woman or girl in a wheelchair.  She hadn’t been present earlier, and she didn’t look familiar.  I wasn’t sure, but she may have been mentally as well as physically disabled; in any case, she was quite severely disabled. 

   Later, at lunch, I noticed her with two women.  I went over, and, after conversing a bit with the two women who were her attendants, it became clear that this was Leslie, who I had known in college 30 years earlier.  We looked at each other in shock and all but screamed, causing others in the dining hall to wonder what was going on.

   As thrilled and in awe as I was by this chance encounter, I was shocked and alarmed by how much more disabled Leslie, who had been disabled very similarly to me with Cerebral Palsy, now was, including in her speech.  It turned out she had been quite ill with meningitis five years earlier.  I also learned that Leslie had been a well-known marriage/relationship counselor and disability activist in Berkeley, was married to a man for 7 years and then came out as a lesbian. She wasn’t taking part in the meeting – she was Jewish – but was there with one of her attendants, a German woman named Ingrid, and her intellectually disabled, teenaged son, Tom, who were attending for a couple days. They, along with another of Leslie’s attendants, had borrowed a van from the independent living center in Berkeley, since Leslie was a member of the center. (While I was off at other activities in the afternoon, David assisted Leslie a bit and got to know her and Ingrid and Tom and was charmed and amused by their relationship. To this day, he affectionately imitates Ingrid’s heavy German accent.)

   This turned out to be quite fortunate – and not just because Leslie said I could stay at her place in Berkeley when I was in the Bay Area.  Leslie and Ingrid et al left the meeting before it was over, but Ingrid offered to borrow the van again and return on the last day, when she took Carl to the nearest train station and returned to take David and me back to my parents in San Rafael.

   Ingrid walked right into my parents’ apartment, sat down on the couch and began talking to my dad, telling him about our encounter at the meeting.  Once again, I was surprised at how easy-going my dad was. Also, my mother was there in a wheelchair.  I tried to talk to her, but she was a bit confused about Ingrid and was having some discomfort.  Once again, David took things in hand and wheeled her back to the nursing unit. 

   At this point, my memory is a bit unclear, but, somehow, there was another rented van which David and I took to return to the hotel in El Cerrito where we had stayed the previous week. I’m also unclear about how another attendant, Virsil, entered the picture that evening or the next day.  I think David remained in the Bay Area to spend time with his family in Fremont, and Virsil and I got onto a train headed to Los Angeles. I don’t remember what happened with the rented van.

   I do remember that the train ride was very long, that I could get a nice chef’s salad on a nice plate and that I cried at one point, overwhelmed by everything that had happened – the accident, spending time with Carl, running into Leslie after 30 years, getting a ride back from the meeting, seeing my mom in the state she was in.  I also had a cold after being out in the chilly, foggy morning on the last morning of Pacific Yearly Morning. 

   Virsil and I got off the train at Union Station in Los Angeles, and then I’m pretty sure we got on a Metrolink train and got off in Claremont and walked the last few blocks to my house.

No one way forward

 

   Here is my latest column in the Claremont Courier.  I wrote it in early December, and it came out on Friday.  I was asked to limit my column to 700 words – a daunting and probably good challenge/exercise. 

               FINDING A NEW LIFE, ALONG WITH THE OLD

       Wait.   Is it okay for me to be doing this? 

   Is it okay for me to be out here on this nice, crisp Fall day?  Am I supposed to be this far from home, on my own, in my wheelchair?  Am I supposed to be going home from the colleges by myself, going along with all the students walking and skateboarding by, instead of getting a ride back? 

   I kept hearing all this, all these questions and precautions, in my head this Fall.  I would get dropped off at a lunchtime talk at the Athenaeum at Claremont McKenna College or a Friday noon concert at Balch Auditorium at Scripps College and say I would get home on my own when it was over.  As much as I loved this, this freedom, these questions kept coming up.  Something was wrong. 

   This wasn’t part of the plan.  This wasn’t supposed to be part of my new life, the new life I set out to find after a spinal surgery left me much more disabled, now almost six years ago.  Yes, I was up in my wheelchair, getting out and about a bit on my own, definitely no longer bedridden, but there was also no way I could get around all over town and beyond in my chair on my own like I used to. 

   So what was I doing, doing what I did in my old life, before the surgery? 

   I had told myself after the surgery, after a year of recovery and getting back up into my wheelchair (actually a new one, designed for my new limitations), that I couldn’t do what I did before and had to find, had to embrace, “my new life.” This meant going a few blocks around my house in my wheelchair, occasionally to the Village if I felt up to it. More than that, it entailed seeing how often I could handle going out to concerts, plays, talks, movies – all the stuff I had always loved doing.

   I was just getting into this venturing out when the pandemic hit.  Suddenly, in March, 2020, I was back stuck at home, more or less.  I wasn’t bedridden again, and, thankfully, I could go out for strolls in the neighborhood on my own (masked, as most of us did outdoors then), but, otherwise, no more venturing out. 

   For me – and for everyone else.  This time, this strange, most unusual time, I wasn’t alone in being stuck at home.  We were all in the same lock-down, if not forced convalescence boat. 

   I confess that I secretly enjoyed it.  I didn’t feel so alone.  And now, perhaps, people would get an idea of what I went through or was going through. 

   Now, as we literally stumble our way out of COVID as it’s unclear even that it’s time to do so, I’m picking up, ever so carefully, sometimes the only one with a mask on, where I left off, continuing venturing out into my new life. And, again, I’m not the only one in this venturing out, figuring out how far is too far, how much is too much.

   These last few years have been a time of reassessment, welcomed or not.  Many of us have drawn new lines, marking off what we want and don’t want in life, what we are and are not willing to do. (Hence, the “great resignation,” etc.)    

   I’m finding out that, while, to my dismay, it hurts too much to wear my high-tops and it’s too difficult to wear my overalls everyday, I can wear my cool wool hats after having my hair cut very short and the headrest on my wheelchair, which I discovered I don’t need, removed.  Not only do I enjoy wearing these almost-forgotten hats, it turns out they enable me to go out in my wheelchair on cooler days, on the beautiful Fall days that I love.

   Yes, things have changed and I have changed, like we all have.  But that doesn’t mean everything has to change.  Yes, I have a new life, a new life that, as I’m learning, can include parts of my “old life” if I take care and, in so doing, be all the richer.

 

An inconvenient sign

   There were signs posted at each check-out stand when I went to the market yesterday.  Big news! 

   “This year, Stater Brothers is giving time off to its employees so that they can enjoy time with their families.”

   So what does this mean?  The sign went on to note the special Thanksgiving hours: Wednesday, November 23, 7 a.m-11 p.m and Thursday, November 24, 7 a.m-5 p.m. 

   Gee.  Thanks.  Employees get to get off at 5 to rush home and likely enjoy a piece of pie with their families and maybe eat a plate of warm-overed leftovers before crashing after working so hard in the rush of people preparing for the big meal.  That someone else made because they were working, maybe until 11, the night before.

   Like I said, gee.  Thanks. 

   Is spending money so important that the market has to be open until 5 on Thanksgiving?  And this is closing early!  Does the market have to be open at all on Thanksgiving?  Would we all go crazy and fall apart if the market was closed on Thanksgiving? 

   Can’t we be sure to pick up that extra cranberry sauce or that last bottle of sparkling cider before Thanksgiving?  (I suspect we would if there was no choice.) Isn’t this why the market is open until 11 on Wednesday? 

   And what if the market closed early, say 5, on Wednesday – so that employees can get home at a reasonable hour, rest up and really enjoy Thanksgiving with their families? Would it be the end of society as we know it?  (Maybe a good thing.) Since when did convenience, our convenience, become so important, paramount? 

   It was clear that it is all about our convenience.  Not only is the market open until 11 on Wednesday and also until 5 on Thanksgiving, at the bottom of the sign, it said something like, “Thank you for your understanding.” As if we are put out by the store closing at 5 so that employees can spend a bit of time with their families and we are being asked to forgive this.

   Also, it’s as if Stater Brothers just came up with this idea – “this year.” Doesn’t the market usually close early on Thanksgiving? 

   And why does it need this explanation?  Why not just say, “We are closing early on Thanksgiving?” I realize that what really bugs me about this sign is that it’s an insult. It’s an insult to the workers, because it makes it look like it’s their fault the market is closing early, causing inconvenience for us, due to their perfectly understandable needs, if not rights, to rest, to spend time with loved ones, to have and enjoy time off.  It’s also an insult to the rest of us, or it should be, because it shows and makes us feel guilt for how much we expect convenience.