SO WHAT HAPPENED?

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Eleven months ago, with bravado I didn’t quite feel — I posted, with an exclamation point: “You’re Never Too Old for Adventure!”  Readers liked it. Liked, liked, liked it.  Although months went by without another word from me, the “likes” kept coming. “Good for her!” they were probably thinking.  “Never Too Old!” is in the same category as “Never Say Die!” and “You’re As Young As You Feel!”  Who wants to quarrel with that?

It turns out I was wrong. You can be too old for adventure, at least the kind of activity that normally passes for adventure.  In your head, you may still feel thirty-five. But you’re not.  You realize it as soon as you assess the world into which you still want to plunge like a youngster. Your body doesn’t know from thirty-five anymore.  It starts looking around for a chair by mid-morning. As for “Never Say Die!” – who’s kidding who?  Come on now.

During the eleven months since “Never Too Old!” I ‘ve had to come to terms with the idea that I’m not just “getting old” anymore.  I am old.  Geriatric medicine has categories. You’re “young old” while you’re between the ages of 70 and 85. After 85? Biologically speaking, you’re “old old “ – at least in comparison with other people. (And who else is there to compare with?)  Disregarding all that, I defiantly squeezed an extra year out of being “young old.”  Although I crossed the biological line into “old old” two months after Bill died; immediately afterwards, I sold a condo and bought a new apartment all by myself. (No, my children didn’t help. They were quite sure I could manage, and I could.) Then I went off to Dublin a couple of months after my 86thbirthday.  I looked pretty good.

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Age 86 in Dublin, September 29, 2017

Yet much to my surprise on reaching Dublin, I found I had aged out of interest in organized travel.  I used to feel I had to see everything important in the world that I could afford to get to.  Now I discovered I didn’t. You might think I’d given up, but I really didn’t want to hurry from one cultural treasure to another anymore.  I didn’t relish spending an hour in a hot crowded museum looking at hammered gold necklaces made by pre-Celts, or going to rather amateurish theater featuring adorable young Irish wannabe thespians in their early twenties just because drama is one of the three or four things you travel to Ireland for. There were too many churches and monasteries and castles and estates of the Anglo-English rich filled with opulent furniture for cranky old me. I had the feeling I’d seen it all before, in other countries at other times.

What I liked best was running into Joe Biden in the gift shop of Trinity College with another member of my travel group. (He carefully ascertained which states we were from — blue, of course — before giving a hug, a photo op, and an admonition not to despair.)

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Don’t look at me, look at him!

I also enjoyed the half day of unscheduled time, which I used to amble alone at my own geriatric pace across the Liffey and up Grafton Street to St. Michael’s Wood. I stopped where I wanted (bookstore and dress shop), sat where I wanted (on a park bench), and ate what I wanted (takeout salad from “Chopped”).

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Crossing the Liffey.

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Walking up Grafton Street.

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Lunchtime at St. Michael’s Wood.

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The Dublin lunch for me.

Then I came home – wishing I’d swallowed my pride, caved, and asked for a wheelchair in both airports instead of dragging my carry-on through inspection and miles of corridors all by myself, as I used to do. And soon  – right after Thanksgiving – a first for me came out of the blue:  a-fib, aka atrial fibrillation.  It was the persistent kind, that doesn’t go away on its own. My heart began beating wildly and quickly. This sounds romantic; it wasn’t. I was always out of breath.  I could have died of a blood clot at any time. My internist thought the cause was eating too much pickled herring over the holiday. The cardiologist dismissed the herring theory; he surmised it was because I had sustained two separate colds with different symptoms one after the other just before Thanksgiving.  But whatever the cause, they both announced (without tact or euphemism) that this can often happen “when you’re old,” and agreed I must hurry over to the hospital that very afternoon, stopping off at home only to arrange care for the cats. “Just for four or five days,” promised the internist.

I was in a hospital bed for over three weeks. Really in it. No hopping out to go to the adjoining bathroom. Bells and whistles went off whenever I moved too close to the mattress edge, even inadvertently — bringing frantic nurses admonishing, “No no no.” What happened to the “four or five days?” It seems that during the TEE (transesophogeal echo) performed to ensure there were no clots near the heart before proceeding with  cardioversion, an a-fib corrective procedure  — my heart rate dropped from crazy high to zero. For a nanosecond I was technically dead, although anesthesia prevented me from being conscious of what it is like to die.

The hospital doctors decided I had been unusually sensitive to the anesthetic.  That may be debatable…or not.  Who knows?  My own cardiologist — whom I credit with saving my life on the spot and keeping me alive during the ensuing three weeks it took to bring me out of congestive heart failure — assured me no oxygen was lost. (Meaning no loss of intelligence, ha ha.)  But now I know what it really means, and feels like, when ER doctors on television shows cry out, “Intubate!” They mean they’re going to shove a thick blue tube down the throat of the patient, preventing speech, swallowing, even screaming. There was also a catheter,  the aforesaid confinement to bed (initially in intensive care), and an extremely unattractive thirty-five pounds of water retained during all this which had to be taken out of me, slowly, with strong diuretics and bedpans that kept me awake all night. They also gave me a pacemaker – which involved another “procedure.” It was inserted, again with an anesthetic, near the surface on the left side of my chest.  It will prevent my heart rate from ever dropping below sixty again. Every time I take my clothes off I can see it, looking like a Zippo cigarette lighter with wires tucked just under the skin. It – or its successor – will be there for me to look at all the rest of my life.  Lest I forget what’s keeping me alive.

I got out of the hospital at Christmas – with a walker, and then a cane, still in a-fib and wobbly. I then spent the next fifty-six days at home on Eliquis, a very strong blood thinner, until it was deemed safe –meaning no further danger of clots — for me to go back to the hospital to have another try at the cardioversion which would shock me out of a-fib.  It did. You could say I got my heart back on Valentine’s Day.

There followed another two months of learning to walk on my own again, and struggling with a particular anti-arrhythmic called amiodorone of which it is said, “Your doctor believes the benefit outweighs the risks.”  What they mean by “risks” are unpleasant to dangerous side effects.  During the period I was taking it I had increasing vertigo, uncontrollable tremors in hands and legs, and a foggy brain. I walked like a drunk. I was afraid to step down a curb.  I even fell. The fall persuaded my cardiologist to let me stop taking it; a fall is the almost worst thing that can happen to an otherwise okay old person. In exchange I had to promise to measure my waking heart rate every morning before getting out of bed. (There’s a little machine for this called an oxymeter; I don’t have to count out loud.) If it’s ever over 100 I must let him know at once.

Alas, amiodorone has a half-life in the body of fifty-six to a hundred or more days.  In my case, it took nearly three months to clear. I could tell by the ebbing of the vertigo when I got up from a horizontal position or got back into bed from standing up, and also by my increasing ability to walk a relatively straight line. I think the half-life has finally expired.  But that also means the chance of a-fib returning has risen from 10% when taking the amiodorone. to 50% now. I knock wood, and keep my fingers crossed.

By the way, don’t think it’s over. The pacemaker has to be checked every three months to be sure it’s working.  I also now need to take five medications a day (although not amiodorone, thank God), three of them twice a day (including the Eliquis). They don’t bother me particularly, although one of them does slow me down.  My brain says, “Move!” and I can’t, because something in the body holds back. Moreover, the costs of the non-generic meds have pushed me into the doughnut hole this year, where I’ve never been before. Only Americans over 65 with Medicare Part D insurance for the price of pharmaceuticals will understand what this means.  Once you reach the doughnut hole you’re on the hook for 45% of the cost of your medication for the rest of the calendar year (until you’ve spent $5000 on your own), despite  substantial monthly premiums. One of mine (Eliquis), which you see advertised on the evening network news quite frequently in the United States, costs $1,100+ without insurance for a three-month supply. They don’t mention that in the commercial. But that’s another post.

Oh, I mustn’t overlook my jolly internist – the one who blamed the a-fib on too much pickled herring; he says that at my age (that word again!) it takes a year to get back the strength lost from three weeks in bed. Of course you don’t just wait for it to come back. You have to exercise, keep moving. God forbid you spend a day just reading, or writing, or lollygagging around.

It all keeps you aware you exist only as long as one small, tired 87-year-old organ goes on valiantly beating – with lots of medical and pharmaceutical help.  I never felt particularly vulnerable and fragile before. Now I do. Which hasn’t stopped me from making new plans.  But still…. It’s a different universe I inhabit.

Why didn’t I blog about all this while it was happening? Well, for one thing, I didn’t know how it was going to come out.  For another, until recently I couldn’t.  In bed, shaky hands, foggy thoughts?  Really?  But now we’re all caught up. If I ever figure out how to change the name of ‘The Getting Old Blog” to “On Being Old,” you’ll understand why.

NEVER TOO OLD FOR ADVENTURE!

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Am I still up for adventure? I’m about to find out.

I haven’t been overseas since 2009. In 2010, I had my right hip replaced during peak travel months. (The hip decided the timing, not me.) For much of 2011, Bill wrestled with erythromelalgia, a  rare nerve disease of the extremities — in his case feet.  It causes extreme pain and you don’t want to get it. Thank God it’s intermittent. All we both hoped for that year was for it to go away, not for us to go away. In 2012 and 2013 came more physical deterrents of one sort or another, none fatal but none travel-friendly. And then his asymptomatic pulmonary fibrosis developed its symptoms, which put the kibosh on any kind of intercontinental movement, even if we had wanted to go in such gloomy circumstances.  But now it’s 2017, my passport’s good, and I’m off tomorrow — age 86 — for seven days of a sponsored program in Dublin, to discover what I can still do.

Why Dublin?  Because (1) it’s one of the very few short programs in the Road Scholar brochure marked “Easy.” Baby steps to begin with. And also (2) I needed a euro country, preferably one where I hadn’t been before.  When downsizing last year, I found inside Bill’s old wallets and mine 380 euros left over from all the lovely summer and autumn traveling we did together in Greece and France and Italy and Portugal.  Every year when our holiday was over, we would bring euros home as a magical promise to ourselves we were going back.  These last ones certainly aren’t accomplishing anything languishing inside my passport case inside a bureau drawer. They need to be where they can do their business.

I had forgotten going away takes such a lot ofpreliminary work (and dollars). But now I’ve arranged for cat care and plant care and being driven to the airport and back… and had my hair cut (and colored) and toenails done and did my own fingernails and notified family and the front desk downstairs as to my coming whereabouts and how to reach me…and broke in a pair of ankle-high wine-colored leather walking shoes and trimmed the packing list down to whatever will fit in a carry-on — challenging, because it’s not summer weather in Dublin anymore. It looks like if I’m ready to go.

I realize every brochure is partly PR, but Road Scholar usually delivers.  So if you’re curious about some of what I might be doing and seeing starting Wednesday, and if you can read the print below on whatever device you’re using to access this post, here’s what they’ve promised:

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Spoiler alert: no more blog posts till I return and recover from jet lag. Not that I’ve been the soul of regularity in the past year or so.  But I have been trying for a post a week lately. Alas, this one will have to do for at least two weeks. However, I shall return.

Wish me luck, wish me fun.  

OLD’S NOT ALWAYS BAD

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For cut flowers bought in a shop, these carnations are very old.  Survivors, you might say.  I carried them home two weeks ago today, part of an ill-advised purchase of red wanna-be petunias that were really something else (what I still don’t know), plus these rimmed carnations, plus a large bunch of spiky greens, all of which I disliked intensely once I had managed to stuff every last stem into an oversized container fit for major floral condolence.  I had wanted yellow flowers, or orange ones, and not too many. I had wanted to put them in my own much smaller rectangular glass vase, wanted them to look at home.  Instead what I let myself be talked into was stiff, institutional, fancy. (SeeMeditation on Flowers,” two posts back.).

But after ten days, the petunia wanna-be’s began to shed their red petals all over the glass table top. The spiky green things wilted and yellowed.  The carnations hung on. Time isn’t always the enemy.  Now that I have only the carnations, they seem more orange. And now they do look the way I wanted them to, a little sloppy, a little droopy, just right next to Bill’s orange bowl.

They’re not going to last, I know that. If you look closely, you can see one carnation has given up, its stem bent sharply towards the ground.  Several of the others are beginning to wrinkle. But even if it’s just for now, that’s fine.  Isn’t now all any of us have, even the young who feel they’ll live forever?

For now, there’s also a bonus.  It’s on my other table, in a little vase I’ve had since I was twenty-seven.  That’s fifty-nine years ago.  Old can surprise you.  Hang on.

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PROUSTIAN MEMORY

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Nearly every morning, after filling a small bowl with fresh organic berries, I spread a tablespoonful of raw crunchy organic almond butter on two brown rice crackers while the water boils for coffee. The reason I’m so precise about the amount of almond butter is because almond butter is caloric. Healthy but caloric.

When raw, without added sugar or salt, it’s also surprisingly expensive, which is interesting to consider. Why should doing nothing to organic almond butter cost more than roasting, salting, and sweetening it first? If I were a culturally responsive and critical blogger, I might have posted about that. But as I’ve always been at heart a me-me-me (and mine) person, I have other thoughts whenever I dip the knife into the glass jar of almond butter and spread the measured amount I’ve allotted to myself on the crackers.

It would be easier to keep dipping until I had enough to cover all the cracker surfaces, preferably thickly. However, given that I’m still vain (admittedly with less and less to be vain about, except I still fit a size 6), I don’t do that. Instead, I try to get as close to the edge of the crackers as possible with the almond butter available on the knife, carefully scraping it thin and out with the blade.

And then nearly every summer morning, rising out of the depths of me as I wield my knife, comes a picture of a narrow-boned slender young woman of perhaps twenty in a miniscule bikini. There’s no extra flesh at all — does she ever eat? — yet you couldn’t call her underweight. She is perfect for her purpose, whatever that may be. She has deeply tanned Mediterranean skin and long nearly straight dark hair. She sits dockside under a café umbrella with two dark men in the sparkling port of Leros, a Greek island in the Dodecanese between the Greek mainland and Turkey. Are the three Greek? Italian? (This part of Greece is a summer getaway for many Italians.) The sun is high, the water — just yards from the café — a saturated gorgeous blue which makes anyone who’s ever seen it long to be back in Greece again. The dark men, in stylish sunglasses, are shirtless; they wear only shorts. Leather slides dangle from their bare feet. They have tangles of dark chest hair, dark straighter hair on arms and legs.

I can’t see her face because she’s bent over two thick slices of warm Greek white bread on a white plate; she’s preparing the bread for one of the men. He’s twenty-six or twenty-eight. He must know she’s doing this for him; he doesn’t touch the cup of bitter black coffee that was part of his order. He’s talking with the other man and smoking while he waits. I can’t hear them well enough to make out the language. As is customary, the bread is served with a lump of butter and a small cuplet of Greek honey. Her hair falling over her face, the young woman spreads the butter slowly and meticulously over the entire warm surface of both slices, until the bread is thinly covered all the way to the soft crusts.

Then she begins again with the honey, teasing it out patiently and slowly over every bit of surface of now melted butter. And again. And yet again. What is this all about? Is it what he expects of her? What she feels is fitting for him? (God forbid a morsel of un-honey-buttered bread enter his mouth?) Why not order more honey? Because he’s the one who’s paying and might not like her not making do? None of this breakfast is apparently for her. And he seemingly ignores her. Not even a friendly pat of thanks. The other man nods, rises and leaves.

We have to leave too. We came to Leros earlier this morning from Lipsi, an even smaller island where we’re spending the summer, to pick up some prints made from a memory stick sent with an acquaintance the week before. Now the noon Flying Dolphin is coming into harbor.  It will soon turn around for the return trip to Lipsi. No waiting for stragglers.

I hadn’t thought about that young woman for a long time. Then I discovered almond butter. Now suddenly, more than ten years later, she comes to me in the mornings as I ply my knife out to every cracker edge, just as she did with the honey. What was their relationship back there on Leros, the dark man with chest curls and his lean subservient handmaiden? I don’t want to think she was just for fun. I like to imagine he had brought her to Leros for a week or two to get her away from some laborious, repetitive job, either in Athens or Naples, because in his way, whatever that was, he cared about her. I want to think they had some kind of relationship; her body wasn’t quite beautiful enough for her to be just arm candy. At other times, on other islands, we saw vacationing men with gorgeous, scantily dressed young women brought along to the beaches to have their luscious glistening near naked flesh everywhere shamelessly palmed and squeezed and fondled, day-long foreplay on public display.  Then when the sun went down, these beauties were fed, doctored with alcohol, and taken to bed, where presumably whatever skills they had, if any, were put to use behind bedroom doors. These young women did nothing all day but lie extended on the sand on their stomachs, idly turning the pages of the same magazine over and over, apparently without shame at their soft supple bodies being so openly degraded by idle male hands, like large pieces of silly putty without feelings.

I hope my young woman wasn’t like that. She’s in her early thirties now. If he didn’t marry her (or she decided in the end she didn’t want him), I hope she found someone else. I also hope she eats now and then, and that whoever she’s with talks to her and loves her. Anyone so dedicated to making two slices of warm white bread as perfectly appetizing as possible, given the limited resources available, deserves at least that, if not more.

You might also wonder why another woman, this one in her seventies, who was sitting near the water in a Greek café while waiting for the Flying Dolphin to take her back to another island, would be so focused on a young woman more than fifty years younger as she buttered bread and spread honey on it. I can only speculate. Because I never had a body like hers? Because dark Mediterranean men with curly chest hair had never looked at me, even in what might have been called my “prime?” (Whether I would have wanted them to is another question.) Because I’m always interested in food, even when I might not let myself eat it because it’s bad for me, has no nutritional value, etcetera etcetera? Or just because I’m always watching other people, listening to them if I can get them to talk, trying to learn something more about life and how we live it, each in our different way, before my own comes to an end? Whichever it was (or all of them), it has now led to me having Proustian memories in the kitchen nearly every morning.

It would be a lie of omission if I didn’t add that when the young woman on Leros comes to mind while I’m putting almond butter on rice crackers, those hot, bright blue and white summers on Lipsi also rise up, almost as alive as they used to be. As Proust observes about the effect of dipping a petite madeleine (a little fluted French cake) in a cup of limewater tea such as his Aunt Leonie gave him as a child when his family brought him from Paris to visit her house in Combray:

And as in that game enjoyed by the Japanese in which they fill a porcelain bowl    with water and steep in it little pieces of paper until then indistinct, which the   moment they are immersed, stretch and twist, assume colors and distinctive           shapes, become flowers, houses, human figures, firm and recognizable, so now all        the flowers in our garden and in M. Swann’s park, and the water lilies of the          Vivonne, and the good people of the village and their little dwellings and the    church and all of Combray and its surroundings, all of this, which is acquiring         form and solidity, emerged, town and gardens alike, from my cup of tea. [From Lydia Davis’s translation of Marcel Proust’s Swann’s Way.]

It seems almond butter – organic, raw and crunchy – is my petite madeleine. I once wrote a first chapter of what was going to be a novella about Lipsi. It was called “An Island of Their Own.” (I did cast it in the third person then, but now there’d be no need that. Almost everyone who’d be in it is either dead or doesn’t read English.) And that was before I discovered almond butter. Maybe I should resurrect it and continue. Not a promise. But I’m not stopping the almond butter in the foreseeable future. So who knows?

MEDITATION ON FLOWERS

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I bought myself some flowers...to cheer myself up..I was the one who bought them. It wasn’t an impulse purchase.  Last Sunday afternoon, I deliberately walked to the flower shop a few blocks away.  So how could this large arrangement of fresh flowers feel so wrong when unwrapped and on the coffee table?

I never used to buy myself fresh flowers. Before Bill, I was working in downtown Boston all the time, and nowhere near a florist. I certainly could have picked up reasonably priced bunches of multi-colored flowers at my suburban supermarket on weekends just before checking out with a cart of groceries. But they somehow always looked unreal to me, and cheap.  Besides, when would I have enjoyed them, or even have had time to change the water? I always seemed to be at the office.

 Afterwards, it was Bill who brought them home.  Always for birthdays and holidays,  more often for no reason at all.  In fact, it was unusual for there not to be a clear glass vase of fresh flowers on the coffee table in the family room where we spent most of our time when downstairs.  (The clear glass was my choice; I disliked opaque containers for fresh flowers.)  When they began to wilt, my frugal tendency would have been to nurse them along a little longer. He would insist on throwing them out. Then he would add “Buy flowers” to his daily list of things to do.

 He especially loved sunflowers.  If they were out of season, he chose lilies, preferably yellow or orange ones.  He never really spent a lot. Three stems, or even two, would do for him, with as much greenery as he could persuade the lady florist to throw in for free. (He had a way with ladies.)  When very occasionally persuaded to bring home roses because they were more romantic, they were yellow.

 My favorite color is red.  (You can see it in the chairs we bought together.  He chose the designs, I chose the reds.)  This made for a certain amount of mild dispute about flowers.  Once he did yield: a dozen red roses on my birthday.  I received them with great enthusiasm, hoping to encourage repeat performances.  No such luck, even though I generally expressed somewhat less warmth than he would have liked for all the yellow, or orange, or yellow and orange it fell to me to arrange in one of our two clear glass vases.

 As for the sunflowers, when we began life together they were my special bête noir.  I had never liked the ubiquitous Van Gogh that shows up in all surveys of French nineteenth century painting. And I particularly disliked the large brown centers and short little petals of the sunflowers themselves. They just didn’t look flowerlike to me.

 Unfortunately, at various times — either before he met me or surreptitiously afterwards — Bill had acquired about twenty stems of artificial sunflowers. They were to tide him over, I suppose, during those periods when there was a dearth of live ones.  Some were close replicas of the real thing, down to the big green leaves.  Others, more fanciful, were white and red, as well as yellow, with larger-than-real petals and colorful smallish centers.  He also had a secret cache of objets d’art in the depths of his large office closet, from which he produced three containers in which to put nine of the fake sunflowers. (Three, three, and three.)  These, after much discussion, found their way into our bedroom, to the top of the piano, and onto a sill in his office. Some of the others   appeared in the finished basement in still other containers I’d never known he had, although we’d been together for over eight years at that point.  The remainder of his sunflower stash I found thrust into the back of that capacious office closet when I was staging the condo to sell it; they were still waiting their chance to come into the light.

 It should come as no surprise I kept them all after he died.  Death changes the value of everything.  In retrospect, I was sorry I’d made a fuss about them.  It wasn’t such a big fuss, but still.  How much I would rather have had him back with all his nutsy sunflowers, actual and artificial, than live alone in a sunflower-free apartment!

 Bill’s fake sunflowers are therefore flourishing again at WindrowsThree sit in my office window:fullsizeoutput_c08 Three are on the bureau next to what I still think of as “his” side of the bed:Bill's sunflowers in the Windrows bedroomThree of the most fake adorn the all-purpose table in what the Windrows architect  designated as the “dining” area:fullsizeoutput_c0a The rest are stuffed into a red (yes!) vase that sits in the living-room window:fullsizeoutput_c0c But even with all the manmade sunflowers artfully placed here and there, up until last week my “new” apartment (not so “new” anymore) still had no fresh flowers in it, if you don’t count the two white orchids given to me on my most recent birthday by people I’ve met only in the last year. Yes, I put the orchids on my living-room windowsills away from direct sun, and yes, I keep them going, as recommended, with three ice cubes in each pot once a week. But to me they’re something else:fullsizeoutput_c0fArt objects maybe. fullsizeoutput_c0eNot what I think of as “fresh flowers” though.  And what’s a home without real flowers?

 About some things I’m quick.  About others not. A while ago, during a burst of sporadic early morning exercise, I passed Monday Morning, an upscale flower shop in Forrestal Village a few blocks from where I live. In the window sat a huge water bucket crammed with bunches of large-faced sunflowers, their big brown living centers turned avidly in the direction of the sun.  $7 a bunch. Instead of going right into the shop as Bill would have done, I walked on by, with a smile of course – thinking how he might have run amok inside and bought two or three bunches.  (One summer he gave my older son a dozen huge sunflowers in thanks for having invited us to visit in Southampton. It was hard to find a vase large enough to accommodate them all in the rented summer house.)

 It took me two weeks of staring at the empty surface of the black glass table in front of the sofa. That was two weeks too many. By then only a few bedraggled sunflowers with little faces remained drooping in a small bucket at the back of Monday Morning, far from sun. Poor sunflowers. (I know: pathetic fallacy.)  And now they were priced at $5 a stem, a deal breaker.

 But I had come out for flowers and I’m stubborn. So what did they have in the big window water bucket this week? There was a twenty dollar bill and a credit card in the back pocket of my jeans and I wasn’t going back with nothing.

 What they had, in more than one bucket, were bunches of red blooms that looked to me sort of like petunias but weren’t. That tells you how much I don’t know about flowers. Almost everything looks like petunias to me. Except sunflowers and lilies and orchids. (And pansies and daisies and carnations: I know what they look like too.) There were also bunches of carnations in all colors, including not only red, but yellow and white and red-rimmed cream.  And also many bunches of greenery, some in thick-leaved silvery green, others with dark green spikes and feathery fronds. $10 a bunch; 3 bunches for $20. All very fresh and perky.

“What color do you like?” asked the saleswoman, closing in for the kill.  “Her chairs are upholstered in red,” said a Windrows acquaintance helpfully; she had come out with me for the walk to Monday Morning and was now putting in her two cents.

I kept eyeing the yellow carnations“Can I mix yellow with red?” Bill had always said you can mix anything with anything, and I always disagreed.  Except now death had intervened.  “Not really,” declared the saleswoman decisively, ending discussion.  “Try these.”  She pulled from the water a bunch of red-rimmed white carnations and pressed them against the bunch of dripping wanna-be red petunias she was already holding.

“Isn’t that nice?” she asked rhetorically.  “It will go perfect with your furniture.”  Really?  What did she know?  But it did make a third bunch of the spiky greenery free. And the greenery might help the flowers.  And the carnations were a kind of orange.  If you squinted.  I wielded the credit card, the acquaintance peeled off for a cup of coffee,  I walked back to Windrows alone with a tissue-wrapped armful.  Literally an armful.

 Which meant I now needed a very large glass vase. There was one, at the back of a high kitchen cabinet, which had come into my possession fifteen months before, when Bill died. It then contained an expensive condolence arrangement.  Bill wouldn’t have liked this vase, even if condolences on his death had nothing to do with it.  It was beyond large, and had a “fancy” shape.  As I trimmed each stem and placed it in the vase, trying to mix red-rimmed carnations with red mystery flowers, I knew the whole enterprise had been a mistake.  Why had I bought so many? Why had I listened to a saleswoman who didn’t know what was in my heart? Did I even know what was in my heart? What was it I really wanted? By the time I had forced the spiky greens in around the edges, and placed the completed arrangement in the center of the black glass table (see top of post), I was hating it.

 Maybe it would look better if I sat on the sofa?  Not really.  fullsizeoutput_bedHow could I make it look the way fresh flowers used to look on the family room coffee table before Bill died?   I moved the vase off center and considered:

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(Sophie had no aesthetic opinions to contribute here. However, as I had awakened her with all my fussing, she was plainly planning to taste the flowers when I finally went away and left her in peace. As there’s never any way I can stop her from doing most of what she wants to do, and since I was already disheartened by my purchase, I had no problem with her plans.)

The table was just too bare.  In the condo, there used to be a large shiny black ceramic bowl that looked like a giant ashtray on each of our two coffee tables, one of them next to the glass vase that held the fresh flowers of the week. The bowl in the family room had a bright yellow inside surface and the one in the living room a bright red inside surface. Occasionally Bill would switch them around — “temporarily,” he said — to see if they looked better that way. I didn’t really care which was in which room as I privately thought they were both extremely unattractive (although clearly some designer’s idea of decorative “art”) and hoped for a long time, without success, that they would fall out of favor when Bill acquired something new that needed table space.  It goes without saying I got rid of them both when downsizing.  Now my eye was missing them.  Why hadn’t I kept at least one?

What I had kept were two small black bowls of his — partly because they didn’t remind me of ashtrays but mostly because they didn’t take up much space. One was lime green inside, the other orange.  I put the orange one next to the oversize vase of red and red-rimmed flowers and pushed it around a bit until it seemed to settle itself on a diagonal to the vase.  It was much smaller than the shape in my memory, but it was all I had. Maybe with Bill's orange dish near it?To cover more table top, I added a third object — my black-bound Kindle, representing the piles of books that used to accumulate wherever Bill was sitting.

A little more mess? And the flowers pulled up higher?

Then I pulled the flowers out of the vase as far as I could — to give them air and free them up a bit.

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Bill would have said, “Enough already.  Leave it.  It’s fine.” And he’d have been right. This was as good as I could do. Let’s face it: I’m neater than Bill ever was.  I can’t leave messes of books and papers around, even to simulate the feeling that he’s still here.  My books are on shelves, my papers in files, magazines in magazine racks.  I was ying, he was yang.  Or vice versa.  That’s why our flowers looked the way they did. And why mine look like this now that he’s gone.

The bottom line here?  When these have lived out their natural life, I’m buying more. No one’s going to talk me into red ones next time. I’m going for yellow. Not necessarily sunflowers, although I’m not ruling that out. And definitely not too many, even if “many” is a bargain.  They’re going to have to fit into one of my own two much smaller rectangular glass vases.

Next time I’ll also know that buying flowers, even yellow ones, won’t be like bringing him back for a while, or making the place where I live like home.  It’s just as close as I can come to it. And that’s something.

 

 

FOR CAT LOVERS: SIX SMALL WAYS TO BE HAPPY

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These six notecards turned up in the gift shop of The Mount, Edith Wharton’s home in the Berkshires.  They’re all from The New Yorker, which means they have nothing to do with Wharton, or The Mount, or its gardens, or my trip to the Berkshires — except that I bought them in The Mount’s shop.

So why were they there? Because Wharton advocated finding happiness in small ways? (See previous post for details.) That would be a very good reason, although it probably isn’t the reason. I’m sure a baker’s dozen of these small pleasures were in the shop because they sell.

They sure got me. When I saw them, I couldn’t not smile. (Of course I also thought, almost at once, “Blog!” Which opened the purse strings even if I’d had more self control.)   My apologies to dog people.  What can I say?  I have cats?  But you know that already.

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EASIER SAID THAN DONE

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One of the “attractions” we visited last weekend during a short trip to the Berkshires was The Mount.  (I say “we” because I went with a relatively new acquaintance from Windrows who had proposed the trip and volunteered to do all the driving, which was about 3 1/2 hours each way from Princeton.)

The Mount is the house the novelist Edith Wharton designed and built in Lenox, Massachusetts, and occupied most of the time from 1902 until 1911, when she separated from her husband and moved to Paris.  It is white and cool — important in the sweltering pre-air-conditioned New York and New England summers — and sits on raised ground.  In the rear is a magnificent landscape of Italianate gardens, formal on one side, “natural” on the other. Although I’d been to Tanglewood, summer home of the Boston Symphony Orchestra in Lenox, several times in my several past lives, I was never before able to visit The Mount because it was under reconstruction each time.   However, for several years now it’s at last been open to the public.

I’m a sucker for gift shops at such places. I always want some little reasonably priced something to remind me I was there.  At The Mount’s gift shop you can buy heavy and expensive illustrated books of Italianate gardens and others about The Mount itself, which I didn’t.  You can also buy copies of most of the over forty books of fiction and non-fiction Wharton wrote and published during her lifetime, which I also didn’t.

According to the guide who led us through the house, she did the writing in bed from 8:30 to 11:30 every morning of her life, before arising to don the corseted, restrictive day clothes of her era. She tossed each handwritten sheet on the floor, later to be gathered and typed up by a secretary.  In her bedroom on the top floor you can see scattered on the bed photocopies of some of those pages — of The House of Mirth, written at The Mount.  The writing enabled her to enhance her inheritance so as to support expensive living in Paris and the Riviera. She was a great success in her lifetime.  (The three novels still generally recognized and admired today, whose titles you may recognize and movie adaptations of which you may have seen, are The Age of Innocence, The House of Mirth, and Ethan Frome).

Not surprisingly, several pithy sayings suitable for printing on cards may be found in the collected works of a woman who wrote so much. Again no surprise — such cards were indeed in the shop, and then they were in my purse, and now they are going to be in the blog.  ($4.00 each: How’s that for a reminder I was there? Ah well, the Mount’s reconstruction is still paying for itself.). Although faithful blog readers may be able to surmise why these two particular cards spoke to me,  I suspect they may have general relevance to most everyone past the first flush of youth. (Or else why would they have been in the shop?)

But first some Wharton back story.  She was born into New York high society in 1862, when women were discouraged from achieving anything but a proper marriage. Unfortunately, she was a bookish girl who read widely (in French, German and Italian as well as English), and early on yearned for a wider intellectual life than was thought seemly for those in her social circle. Her marriage to Ted Wharton was not good.  He was social, outgoing and apparently not much of a thinker; she relished solitude, books, and good conversation. There were no children. Eventually he became mentally unbalanced, they separated, and she achieved a divorce.  She is known to have had only one lover, after separating from her husband; the lover turned out to be a cad with a divorced wife, a mistress, a fiancee, and a propensity for sticking his pen in many inkwells. Nonetheless, she hung on for three years before giving up.  (Her private papers reveal that it was with him, at the age of 47, she had her first orgasm.) Afterwards, she continued her ongoing and copious written correspondence with male friends such as Henry James and Walter Berry, but seemed to have had no later intimates.

As she advises (on the card above), “If only we’d stop trying to be happy, we’d have a pretty good time.”  And perhaps she did have a pretty good time.  (Not to be cynical, but I can’t help thinking the money helped.  However, she earned it herself. And I do believe she enjoyed the writing as well as the spending.) Moreover, I once had a psychotherapist who said just about the same thing.  He asked me what I wanted.  I was fifty-seven.  I said I wanted to be happy. He said happiness was not the goal of therapy.

Another card (which I also bought) quotes Wharton’s thoughts on how to have a pretty good time without trying to be happy.  Actually, the thoughts are not specifically about not trying to be happy, but about how to stay alive — which I take to mean alive in all senses of the word — well after the age at which most (all right, many) people start to fall apart.

But it seems to me it comes to the same thing in the end:

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Be unafraid of change, insatiable in intellectual curiosity, interested in big things?That’s a tall order, about which we could talk for days. For one thing,  life is change.  Often we forget it.  Our lives continue day to day, seemingly the same.  Boring even.  And then, suddenly, boom! — it’s not the same at all.  And yes, it is scary.  Especially the older you get.  But what are you going to do?  Give up?  Or go on?  I’m not going to wax philosophical about intellectual curiosity or interest in big things, either. You’ve got it.  Or you don’t.  (Although I suppose you could force yourself because you know it’s good for you; better to be insatiable about learning something new than be insatiable about chocolate cake.)

But happy in small ways?  Well, sure. Small ways to be happy turn up all the time, usually when we least expect.  In fact, six of them turned up right in The Mount’s gift shop, next to the Wharton lessons in life. However, I’m also discovering that part of becoming old old (“long past the usual date of disintegration”) is pacing yourself.  So I’ll just save them for the next post!

STARTING OVER

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Some readers have expressed interest in where I went after the sale of the condo commemorated recently in a set of self-indulgent photos.  (“As I Was Saying….,” July 18, 2017.)  So this post, equally self-referential, is about where I live now. [Be advised there was no professional photographer at work here this time.  Just me with an iPhone.]

fullsizeoutput_b93When we first saw it together two years or so before he died, Bill thought it looked like a middle-class Miami hotel.  No way was he going to move here. Ever. A year later, when our stairs had become too much of a daily challenge, he capitulated.  We visited several “retirement” communities with apartments all on one floor.  This seemed the best of them, for a variety of reasons I can go into another time.

And it does look better (although still somewhat institutional) when seen from the front door:

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You could even imagine elderly people enjoying the sun, or shade, on one of the front benches near the fountain when they’re not quite mobile enough to get away:

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However, it was at least in part the presence of all those not quite “able-bodied” elderly people — with their walkers, or in their wheelchairs pushed by aides — that put us off.  (As if we weren’t getting “elderly” ourselves.) But eventually the condo stairs — and Bill’s fifty-foot oxygen cannula — got the better of us.  And where would we go if we sold the condo? The reason most persuasive for coming here was the apartments.  Many of them had interesting layouts, quite unlike the rectangular, unimaginative arrangement of rooms in the two other places we’d checked out.  Bottom line: We’d just have to learn to live with all the other aspects of a “retirement” community we weren’t ready for.

Then Bill got too sick to think about moving anywhere.  Until very near the end, just before they put him under with morphine so he could be intubated, when he wrote in a little notebook:  “Get Windrows apartment.” He wanted me not to be so alone after he was gone.  I can’t say I moved here because he said I should.  It’s that I finally decided he was right.  Even if I didn’t look and sound as old as I really was (nearly eighty-five when he died), sooner or later I wouldn’t be able to drag the garbage and recycling out to the curb. Sooner or later, I wouldn’t be able to drive, for one reason or another.  Sooner or later, I might fall. And then who would I call?

Apartments of the size you want become available at infrequent intervals at Windrows.  (Yes, that’s the name of the place.) You have to wait for someone to move nearer their children, or else to die.  But the two guys in the Marketing Department worked with me.  And I was lucky.  I managed to snag a one bedroom with den on the second floor that even Bill would have approved.  Affordable. (Just.) Spacious. Sunny in the afternoons. A porch off the living room.  I also had enough money left over from the sale of the condo to replace the carpeted and tiled apartment floors with wood floors, have everything but the kitchen repainted white, install pleated pull-up window shades plus many more ceiling lights, and switch the cable and television lines from one wall to another, in order to accommodate better placement for the computer in the office, the television set in the living-room wall unit.  So now it’s begun to look like home to me, especially as I was able to find room in it for the “modern” furniture — actually mid-twentieth century furniture — Bill and I bought after we began living together. (Perhaps you’ll recognize some of the pieces and pictures from the condo shown in the previous post.) The two cats and I moved in last September 23.

I try not to think of it as the last place I’ll ever live.  Unlike apartments in most retirement communities, residents here aren’t locked into any kind of continuing-care scheme. These apartments are bought and sold at market rates.   So I can always decide this is not for me, sell, and move away.  Where, I have no idea just yet.  But the possibility is there.  It consoles me, gives me a sense I can still go on inventing my life. Anyway, the apartment is certainly a good place to which I can withdraw whenever community living gets too much for me.

There are miles and miles of corridors.  Four and a half floors of them, each of which takes about ten minutes to circle in its entirety by foot. When you first move in, you need breadcrumbs to find your way back to wherever you came from.  Here’s a small part of the second floor near the north elevator: fullsizeoutput_bb2

But eventually you find the right door, and open it:fullsizeoutput_b98

Front hall of apartment (with Sophie at right):fullsizeoutput_b9b

Better view of living room area: fullsizeoutput_b9c

View from sofa of piano, dining area and kitchen pass-through:fullsizeoutput_ba8

I also managed to find a wall for our expensive Italian folly, the wall unit which had to be taken apart for the move and then put back together:fullsizeoutput_ba1

There’s a mandatory eating plan: one chooses either four, fifteen or thirty meals a month. This is allegedly to forestall reclusive tendencies.  True recluses, or those who prefer to eat at home, can circumvent Windrows’ paternalistic tendencies by ordering one of the prepaid plan meals by 3:30 in the afternoon (a menu is available online, on a special television channel, and printed out in the mail room), and then picking it up downstairs or — for $5 a pop — having it delivered. Be that as it may, every apartment has a fully equipped kitchen.  I had mine painted the same color as the kitchen in our condo, to give me the feeling that at least some things have stayed the same:fullsizeoutput_ba4fullsizeoutput_ba5

The “den” has just about the same square footage as my office (aka the third bedroom) in the condo, although the windows are on a different wall and it has no closet. It therefore serves quite nicely as a more-or-less familiar place in which to work, with the added perk that I get a view of the porch and the tree beyond it when I sit at the computer. The double doors can be closed off from the view of guests. When there are guests. fullsizeoutput_ba0fullsizeoutput_ba6

The oblong red box on the floor was a Danish magazine holder that Bill acquired by mail, possibly even from Denmark!  Alas, once it reached us it never did get to hold magazines, as it filled up too quickly beside his chair with Kleenex boxes, eyeglass cleaners, and various gadgets for now never-to-be-discovered uses.  Emptied and transported to Windrows, it now serves as a place for Sophie to snooze when I’m online and she wants to be nearby:fullsizeoutput_ba7

Looking out at the porch from my desk chair:fullsizeoutput_baa

Heading down the hall, past a second (guest) bathroom, towards the bedroom:fullsizeoutput_ba9

The guest bathroom is sort of a small shrine to Bill.  His bigger Calder mobile sways over the toilet. (It used to be in his office, aka the condo second bedroom.) One one wall is a Hebrew rendering of the Physician’s Oath of Maimonides: “Inspire me with love for my art and for thy creatures. In the sufferer, let me see only the human being.” Behind the toilet is a numbered photograph of Balliol College, Oxford, which Bill liked very much. We had it in the bedroom, facing the bed. The two small framed photos taken at the base of the Acropolis are mine, from the year before we met. But we spent six happy summer vacations on a Greek island together.  And Greece is Greece. So why not hang them here?fullsizeoutput_bab

The bedroom, which is large, is not so different from the bedroom I shared with Bill in the Princeton condo. (Except, of course — a very big “except” — he’s never seen this bedroom, never been in it.  I still keep strictly to my side of the bed, though.  Habit? Hope?)  That’s Sasha curled up in comfort on her two Shaker chairs by the window. She first began to do that, in the condo, when she was a kitten:fullsizeoutput_bac

The lesser Calder is in the bathroom attached to the bedroom. You can tell which bathroom I use the most:fullsizeoutput_bad

Sasha and Sophie use the same bathroom as I do.  The two boxes are not “hers” and “hers.”  They both use the one on the left more.  I don’t know why.  I can switch the boxes but they still favor the one on the left.  The right box only gets the occasional dump.  Even in the interests of full disclosure, do you really need to know that?  Probably not.fullsizeoutput_bb1

I can see the porch from the side bedroom window too:fullsizeoutput_bae

But it looks best when you step outside through the door from the living room:fullsizeoutput_bb6

The two potted boxwoods (one at each end of the railing) were a housewarming present from my older son:fullsizeoutput_bb7  

And the tree conveniently planted outside my line of apartments shields most of the windows from views of the rear parking lot:IMG_2280fullsizeoutput_bb3

It wouldn’t be real life, though, if there weren’t another view from the right hand living room window.  Fortunately, I can’t get too close to it.  The sofa and cat tree are in the way.  So this, less aesthetic, view is best seen by Sasha, from the top of her cat tree.  She finds it interesting.  I find it illustrative of the fact that nothing in life is perfect.fullsizeoutput_bb4

And there, dear readers, I shall leave you for the time being — your curiosity over-satisfied.  What life is like at Windrows once I walk out the door of the apartment, down the carpeted corridors and into the north elevator I shall leave for what will likely be many other posts, although I hope not all of them.

Bear in mind that I am now a recently-turned-eighty-six-year-old malcontent who is not at all happy at having disbelievingly found herself over the border of that far country described by geriatricians as “old old age.”  How could it have happened?  I am going away to the Berkshires for four days tomorrow — plays, Yo-Yo Ma, museums — to forget about it for a short while.  Will reply to comments, if any, when I get back.  

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AS I WAS SAYING (five months ago)….

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Selling a house/condo/apartment takes fakery, the same kind of fakery as selling almost anything else in a market economy, including yourself.  But you read all about faking the “anything else” in my last post. ( “Faking It,” February 2, 2017.)  So let’s move on to profitable unloading of real estate.  Very few people wanting to buy seem to be really clear about what they’re looking for.  Oh, they may say it’s location — location, location, as the realtors are wont to chant ad nauseam. Or square footage.  Or number of rooms. Or a sunny kitchen. Or a good public school for the children.  And it may well be some or all of those things are what they hope for. But when the realtor shows them the location, the footage, the rooms, the sun on the breakfast table (not so easy in itself), they will still dither and waffle and toe the sand and think about it. And think about it. And think about it.  And get back you. Maybe.

For a speedy sale you’ve got to enchant them, open their minds to a fairy tale life:  the life they imagine they could have in your house/condo/ apartment. Of course they never will have that life. Nobody does.  Nobody keeps their kitchen counters immaculately empty except  for one perfect appliance (perhaps a Museum of Modern Art toaster) and a charming French pot of herbs near the window. Nobody’s stove top is free of cooking utensils, except for a little red enamel teakettle. Nobody’s rooms are junk-free, emptied of detritus, piles of this and that on the floor, children’s toys, cat trees, litter boxes. Almost nobody’s bathroom counters aren’t crammed with toothbrushes, mouthwashes, beauty aids, Kleenex boxes, deodorant, Q-tips.

But you can play let’s pretend.  You can be the fairy godmother who transports your potential buyer into never-never land. Of course, it’ll take more than just airily waving a wand to whisk away all the imperfections of real life.  You’ll have to pile the kitchen stuff in the oven, in the broom closet, in the dishwasher.  You’ll have to buy some Sterilite boxes and sweep the bathroom mess into them, for storage under the sink.  You’ll have to clear the tops of your furniture except  for one or two really good decorative objects.  You’ll have to polish those tops till they shine. Into the closets with everything else! Then up with the shades, on with the lights! Let everything be bright and cheery and uncluttered and clean! That’s what modern fairy godmothers do.

I learned about this sleight-of-hand back in Cambridge, Massachusetts in 2005, when I sold a condo all by myself for the very first time. I was beginning to tell you about it in that last post  — published, alas, much too long ago. That was a post designed to set us up (in its “To be continued” promise), for an account of my second sale, which was of the condo Bill and I lived in together for ten years, until he died. That second sale would have the logical next chapter in the ongoing saga of my life after his death. However, the ongoing-ness interfered with the blog. (I won’t explain, except to say there was too much happening at once, too soon, to digest and write about it.)

And now that I’m a year past the worst of it, even selling our home last year has become stale news.  So let me summarize quickly:  The Cambridge sale in 2006 was a great success. I had bought that first condo (two bedrooms, one bath) for $200,000, lived in it for eleven years (the last four with Bill), and sold it (after learning to play fairy godmother) for between two and three times what I’d bought it for.  True, I sold in a rising market.  But still…. There was even a bidding war after the first open house.  Two potential buyers even asked if they could also buy everything in it, it looked so nice, so ready-to-move-into.  (And this “everything” was mostly my mother’s old furniture and knick-knacks, from the 1960’s). With that kind of success, “staging” (aka faking it) was a lesson I didn’t forget.

A couple of photos should give you an idea of what that Cambridge condo apartment looked like in its “wouldn’t it be nice if” fairy-tale period, until the closing:

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Looking into Cambridge dining room from living room (after staging).  Portion of living room in photo below.

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Thus, when it came time to sell the Princeton condo last year, I knew just what to do. In a way it was easier without Bill, although being without him was why I had to sell; we didn’t have to argue about where to put what where.  There was a garage and half the basement for storage (we’d turned the other half into a furnished room); we already had a lot of Sterilite boxes in multiple sizes; and I did a lot of dragging things up and down stairs on my own, to tuck them out of sight. Then the realtor brought in a professional photographer.  He put the camera on the floor. “Why is he doing that?” I asked.  “It makes for better pictures,” the realtor whispered.

It sure did. I may have played the role of fairy godmother to my property; the photographer played fairy godfather.  His camera placement and wide-angled lens turned a modest, nicely furnished condo, now “staged,” into a magical dream.  Who wouldn’t want to live there? Even though I knew how much trickery had gone into what we produced together, I loved his pictures so much I bought a set, to keep forever and forever after they vanished from the internet, post-sale.  Although it never really looked like this when Bill and I lived there with our two British Blue cats (their grey hairs over everything, their litter scattered on the bathroom floors), I could imagine, couldn’t I?  For one shining moment (e.g., ten days), this beautifully spacious sunlit dream house was mine.

There was another bidding war.  I don’t know what the successful buyer was thinking when she offered the slightly inflated asking price. But I didn’t ask. I needed her money to buy myself and the cats a much smaller apartment — one bedroom with “den” (a separate room, although minus a closet) — in an over-55 community, and then fix it up to my liking. (Wood floors, white walls, more lights, etc.) So I busied myself with that.  It’s where I’m living now.  A very different kind of place, and a different kind of life. I’m sure you’ll be hearing at least something about it in future posts.

But I still have the photos of what 35 McComb looked like through the photographer’s camera eye just before its sale. And although I know it’s not really a good idea to keep looking back — I might turn into a pillar of salt  — I do take those photos out from time to time.  So you’ll have to see them too, to dot all the i’s and cross all the t’s. The front door is at the top of the post.  You can leave whenever you like.  I left out photos of the three bathrooms and the laundry room, so as not to overtax your indulgence. But if you do stay till the end of the tour, just remember — this is what “faking it” looks like:

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FAKING IT

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Even as a young girl eagerly devouring the “ladies” magazines my mother brought home from the corner newsstand, I thought the advice I found there about keeping a husband’s interest after marriage quite unfair. Especially the part about hurrying to the bathroom to apply makeup before he woke up and caught you with a nakedly unadorned face.  Although privately agreeing with the magazine beauty columnists that one looked much better enhanced by the sorcery of cosmetics than not, I did wonder how come the man didn’t have to do anything special to keep the marriage going.  Of course this was a long time ago, when in most marriages — as I realized long before I had finished high school — the man earned all or almost all the money and the woman’s job, if you could call it that, was to make sure he wanted to go on supporting her.

Whether a heavily made-up face was what a man fantasized about in the privacy of his side of the double bed is another question entirely, and not within the purview of this piece, wherever you thought its headline was leading.  But even if the magazine editors didn’t quite get the male psyche, they were right on the button with the then-economic interests of their readers. Keep yourself attractive, by whatever standards then obtained. Whether “attractiveness” also included faking pleasure between the sheets even where there really was none was probably determined privately by the woman on a case-by-case basis. In any event, back in those long-ago days when I was still living under my parents’ roof, I thought both parties simply exploded simultaneously with some kind of as yet unimaginable joy upon vaginal entry,  which meant that kind of fakery was not an issue.

When at last old enough actually to share a double bed with another, I never was able to force myself to reach for the cosmetic case before he opened his eyes.  However, time had marched on and that was no longer key.  What you were supposed to be was thin, or thinnish (even if “thin” didn’t come naturally); you also had to wear a panty girdle or girdle even if you were thin so nothing at all could possibly jiggle, so your behind was one unbifurcated cheek (preferably perky), and also so any bumps at the top of your thighs, however slender, wouldn’t show in a sheath dress or skirt. That was just to get to first base with a man — long before the necessity of having to keep his mind on you after marriage.

Ideally, you also had to be able to manage your hair, do without glasses in social situations, be a lady in the living room and a whore in the bedroom.  Of course plenty of women did get to first base without some or all of these qualities (myself certainly included), but most of us nevertheless hated one or more parts of our bodies because they didn’t look the way they were “supposed” to look and therefore struggled with as many fakeries as we could afford. (Hot rollers, padded bras, stilettos that improved the ankles but were killers to walk in, dieting in public but raiding the fridge once the girdle was off for the night; I’m sure every female reader of a certain age has her own list.)  I remember asking both a journal when I kept one, and a psychotherapist when I could pay one, “Why can’t I be loved just for me?”

Indeed, who doesn’t want to be loved just for being who they really are?  And yet long after marriage — or multiple marriages — most of us continue to play games with the truth. If we’re lucky, not so much on the domestic front as we and our men grow older and more realistic about what is important, and lovable. But almost always in the outside world, in order to survive. Although I haven’t worked for pay for over ten years,  I still keep a moralizing magnet on my refrigerator acquired during all those decades of having to market myself to successive employers, latterly at an age which on paper might have looked like the kiss of death: “Good clothes open all doors.”  They do, and they did.  Of course, once the door opens and you walk in, the clothes aren’t enough.  You’ve got to be up to scratch on all the multiple facets of the work you’re applying to do.  But you never get to that if the door never opens.

Bottom line: some form of fakery is probably necessary in a market economy for almost every kind of success.   For instance, as a new late-life lawyer in a large firm I soon learned my professional survival would likely depend on keeping to myself all real opinions about the value of what we were doing on behalf of our huge corporate clients.  Do I therefore owe my legal career, and consequent ability to achieve a modest retirement  before death, to the fact that I had little yellow stickies on my computer and inside my front desk drawer reminding me all day long to KYMS?  (My personal acronym for “Keep Your Mouth Shut.”) Not entirely. Good work was also involved.  But KYMS was an excellent start.

Which brings me to yet another example:  selling residential real estate, where the fakery is known in the trade as “staging.”  I learned all about staging in 2005 while selling the first property I had ever owned only in my own name: a two-bedroom, one-bath walk-up apartment on the second floor of a a semi-historic building in Cambridge, Massachusetts.  The building may have been old, but it did have charm and a good address, and the floor-through apartment had “good bones.”  Moreover, I was basically neat, and didn’t own a lot of crap because I had left most of it in the marital home when I moved out six years before buying the Cambridge apartment.

Then I met Bill.  I had bought the apartment  without foreseeing a second occupant, especially one who collected “stuff.”  Bill brought his smaller possessions with him.  (The larger ones, I learned later, were in storage.) Where to put them?  There was one sizable locker unit two floors down in the basement of the building, but it was already fairly full of beloved old grade school math notebooks and incomplete sets of Clue and Monopoly belonging to my two adult but as yet unmarried sons.  Besides, Bill didn’t really want to be rummaging around in a dark basement locker every time he wanted something.  So any available surfaces of my previously uncluttered home began to look like this:

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Cambridge 2005: End table in den (aka second bedroom). Formerly holding only lamp.

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Cambridge 2005: Other table in den. (Formerly holding only lamp. Big pictures mine; small pictures his.)

Since I wasn’t blogging in those days, I have no photographs of his side of the bed with its cluttered bureau top and piles of books on the floor, or of the single bathroom after it had acquired his toiletries and nutritional supplements as well as mine. However I’m sure you can imagine. (Having the two photos above was dumb luck.) “Great apartment,” said the friendly realtor. “But you’ll have to clear all this stuff away.”

“Where shall I hide it?” I asked plaintively.

“Wherever.” She waved her hand blithely.  “I’m sure you’ll find a place.”

[To be concluded in next post.]

 

 

 

 

STAY PUT OR MOVE ON?

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The conventional wisdom extended to the new widow or widower is to not do anything for a while, or (putting it another way) to do only what you feel like doing.  That’s tricky advice, because of the “feeling” component.  Do you go on living where and how you’ve always lived with the person who’s died — reminded every hour, in that familiar setting you shared, that the person who should also have been there is absent forever?  You may “feel” you want to stay, close to as much of his or her presence as lingers, everywhere you look, in the clothing, the furniture, the favorite foods in the pantry.  However, staying put may also prolong the excruciating feeling your life has been torn in two and the other half remains missing.  Your own (now disabled) life may stay put as well.

Or do you take a deep breath and turn your back on your joint past (without ever forgetting it)?  Do you then begin looking for another, smaller, different place in which to live because you “feel” that’s the only way begin building a life of your own even though you really don’t feel like doing it just yet? Should moving on begin with an actual move?

I present this query as if it were a matter of free choice. Indeed, for all the widows I met in the two six-week bereavement groups it was a free choice.  All had been married to the same man since emerging from college. (“From my father to my husband,” as one put it.)  All had comfortable homes in which they had raised their children and which grandchildren visited frequently, homes now free and clear of mortgages. They drove relatively new and powerful cars. Some had second houses in Florida, to escape the winter months.In no case did money problems figure among their laments.  In other words,  in their bereavement they were well fixed to stay put. And I believe that in the four months or so since the second group disbanded, none of these widows has moved. One who I ran into in the local market hasn’t yet begun to empty her husband’s closet, although he died about a year ago; she says she’s begun to think about it only now because of her daughter’s urging.

Two of us have not stayed put.  F., a recent widower, nursed his artist wife for four years until in the end he lost her to cancer. They had been living in a large house in a township about thirty minutes from Princeton, chosen to accommodate his wife’s studio and artwork. Now she was gone and he was alone with all the memories which seeing her paintings, sculpture and drawings around him every day could only exacerbate. Moreover, he had both professional and social connections in Princeton, from which he was somewhat isolated where he lived. Yet these were the people who might best be able to help him begin again.  So F. put his house on the market within a few months of the funeral and before the bereavement group’s first session.  He also made a deposit on a new one-bedroom rental apartment in the heart of Princeton.  This didn’t mean he had worked through his grief.  He felt, however, that he had a better chance of recovery (if we can call it that) in a new environment with fewer triggers to remind him of what he had lost.

My situation too was somewhat different from that of the other members of the two groups. I also had a choice. But not a good or completely free one.  Bill and I had been together only fifteen years, and although we split all expenses down the middle, I was the one who bought the condo we’d lived in for the ten years since we came to Princeton.  While we kept separate checking accounts, we also shared a joint one, into which last January he had transferred sufficient funds to pay part of his share for the calendar year. But his social security disappeared with his death in May.  Although until 2017 I could carry the condo expenses alone (including mortgage and real estate taxes)  without touching capital, after that I would need to begin withdrawing what I had counted on not needing to withdraw so quickly, since there wouldn’t be any more when it was gone.   That seemed unwise.  Irrespective of my “feelings” about the condo, which reminded me wherever I looked of the other person who used to live there and had vanished, I knew I should sell before 2017.

I knew this as soon as Bill died in May.  It took me about three weeks to emerge from shock, weakness, and very frequent tears. Then V., a real estate agent, called. She wasn’t reading my mind.  I was the one who had first called her mid-April to set up a meeting I had to cancel when he developed terminal pneumonia. She was now following up.

The back story is that for a long time after the symptoms of his disease manifested itself, Bill had insisted he wanted to die at home.  About a year ago, he reluctantly changed his mind.  The stairs were becoming too difficult, given the state of his lungs.  We needed to live on one floor, preferably where many of the chores of home maintenance would be taken care of, and perhaps where there was also access to nursing care if needed. However there could be no buying without selling.  The money for the next place was tied up in my equity in the condo.

At the time, I was ambivalent.  Although approaching my 85th birthday, I didn’t feel ready to consign myself to “a retirement community.”  I thought of those communities as holding pens for death. On the other hand, Bill needed to be in such a place. So I swallowed my reservations. We visited a beautiful and (for us) hugely expensive facility run by the Quakers in Pennsylvania, another in Montgomery  (just north of Princeton) which gave me possibly irrational but nevertheless bad vibes, and a third in Plainsboro (but with a Princeton address), where the lovely apartments were market-rate — and without future medical care built into the monthly fees, thereby greatly raising them. I also began calling real estate agents to get started with the sale part of this double enterprise.  We met with three and were about to meet with V., who would have been the fourth, before Bill became too sick to proceed.

So when V. called at the beginning of June, I could have consulted my feelings and said, “Not yet.”  Or I could have made the choice I thought I should, and said, “Yes come. Let’s talk.”  Not in any way enthusiastic about moving to that “retirement community” (just about the only source of one-floor apartments in or near Princeton not priced out of my league), but driven by financial prudence (as well as fear), I agreed to meet with V. in a week.  That gave me just one  week to rid the condo of all Bill’s medications, cannulas, inhalers, oxygen concentrators and related equipment; to get off the floors, and find a place in the already full bookcases for, the towers of books surrounding every place he liked to sit; and also to make his office (the second bedroom) and his bathroom (the second bathroom) somewhat more presentable.

There’s nothing like a timetable to get you off your ass and thinking again about something other than yourself. Plenty of time to cry early in the morning and in bed at night.  As for the question posed in the headline, in a way (and much like attendance at bereavement groups) it’s different strokes for different folks. What answer might I have given if I were rolling in money?  I truly don’t know.  But I’m not.  That said, I think I made the right decision — for me.  I’m better off, in almost all ways, here than there.

The prospect of V.’s visit precipitated a whirlwind of activity that didn’t let up until after I moved into the Plainsboro residence near the end of September.  By that time I had resumed sporadic, although not yet regular blogging. I had also reaped all kinds of kudos from acquaintances for having rebounded so efficiently and accomplished so much in such a short time. I hadn’t “rebounded.”  I still miss Bill acutely, beyond writing about it,  even in this new environment. But I did accomplish quite a bit in not very much time at all.  However, there’s no mystery or miracle about it.  You do what you have to do.  And with some luck, and some help from friends and interested professionals, it gets done.

One or two (or three) more posts about the “moving on” part. And then we’re up to date!

TALKING ABOUT GRIEF

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Does talking about it help?

There’s no one answer. We’re all different.  The only thing you and I have in common is that we’re both human.  In other respects each of us is, miraculously, one of a kind. So people experience loss of a loved person differently.  The searing pain may be the same in every bereaved heart. There the similarity probably ends.

There are differences between loss of one parent and then of the remaining parent, between loss of a brother or sister and loss of a child or of a husband or wife. Family situations also vary among the grieving survivors.  There may be strong familial support or no family at all, loving friends or none. Often when the survivor of a death is getting on in years, the loving friends who might have been there are already dead themselves.

For the most part, men and women also seem to differ in their response to what has happened. Many men may feel they can tough it out alone, or that their loss is too private to share. Some simply lack the habit of being able to talk about feelings.  There are women who also feel uncomfortable speaking openly about private matters. However, these appear to be in the minority.   In the five or six walk-in bereavement group meetings and two six-week bereavement group sessions I attended after Bill died, I encountered only five men — two in one of the six-week groups and three others at separate walk-in sessions. Three were widowers and two were sons who had lived all their lives with their mothers.  Everyone else I met was a recent widow, or a sorrowful daughter or sister.

Therefore anything I say here about the value of talking about one’s great loss will not be useful for everyone.  I have at least one friend, no shrinking violet, who went to a couple of meetings after her husband died at too young an age and felt bereavement groups would not help her deal with the hand she’d been dealt.   Nonetheless, since I’ve been quite frequently asked why I attended (and now and then still do attend) such meetings, I’m going to set down here my experience with the benefits of going.

At the time Bill died last May, the very existence of bereavement groups hovered only lightly on the periphery of my consciousness as a vague notion they provided spiritual solace for church members. Since I’m not only nominally Jewish but entirely without spiritual faith of any kind, I would therefore not have been in any way comforted by the references to Jesus and God I expected would be offered by such groups. However, on one of his last days of consciousness before the morphine required for intubation knocked him out, Bill mentioned them. Although a psychiatrist by training, he had always favored talk therapy over pharmacology wherever medication might not have been absolutely necessary. Concerned even on his deathbed about my being alone in Princeton after he left me, he tried to think of what might help. So of course his suggestions included a place where I could talk it out.

My own instinct, not dissimilar, was to find a psychotherapist instead of a group — of necessity one who would take Medicare.  Throughout my life, it was always psychotherapy that helped me survive and surmount some very real difficulties.  Afterwards I would say, in jest (but it was also true), “I can’t leave a husband until I have a shrink, and I can’t leave a shrink until I’ve found another husband.”  I’ve also said, not in jest (but equally true), “I don’t know what I think till I hear what I say.”  Last May I wasn’t leaving anyone; he was unwillingly leaving me.  But the default position was the same.  I was going to need someone to talk to.

When I had sought therapy before, I was working and could pay.  Now I wasn’t working, and couldn’t pay — at least not for long.  In the intervening years, it has also become hard to find a therapist (let alone a psychiatrist who still does talk therapy) willing to settle for what Medicare will approve per session.  Eventually, with the help of my internist, I did find such a person. It is a great and much appreciated luxury for someone like me, needing to talk or write about what is going inside, to be able to sit down once a week with someone absolutely supportive and non-judgmental who for fifty minutes at a time exists only to listen and offer an occasional comment or suggestion.  But it took time to find her.  In the meanwhile, there was a nonsectarian bereavement group meeting once a month at the Princeton Senior Center where you could just walk in without registering or making a prior commitment.

I’m not a group person.  I like one-on-one, not only in therapy but with the people to whom I can be open. So it was with some trepidation that I showed up at the Princeton walk-in group on May 16, ten days after Bill’s death.  There were about eight people in the room, plus the group leader, who was a licensed social worker and part of the local hospital hospice staff, and also the hospital chaplain, a young woman newly pregnant. Despite my hesitation at the presence of the chaplain, she said nothing remotely “spiritual” at any point during the hour and a half we were there. Her function was to co-direct the discussion with the leader and, I suppose, to be available with her chaplain hat on for anyone who sought her out privately afterwards.

The group was part of the hospital’s outreach to the community. We sat around a long table on which there was a large box of Kleenex, introduced ourselves, identified the person we were there for and when he or she had died.  That was all we had to say, unless we felt like saying more. Almost everyone in the room said I had come too soon.  I didn’t think so. “Soon” is when you are raw and bleeding inside.  “Soon” is when you most need some kind of triage.  Even if you just listen to other people talk about how they are hurting without saying anything yourself, it helps. It helps to hear you’re not by yourself in feeling such extreme pain and fear. (Some people don’t admit the fear, but you can hear it in what they say.)

A number of acquaintances have said to me they didn’t need groups because when they were in that dark place hollowed out by death they were able to talk to family and friends.  I didn’t find talking to family and friends to be the same.  Even when you’re being deluged with phone calls, and invitations to dinner, and visitors bearing flowers and food, the callers and visitors don’t really want to hear too much about how you’re feeling.  You can sense their uneasiness as you speak. They make sympathetic sounds and nod and offer tissues, and then try to turn the conversation to other things, either to distract you from your sorrow or because they’re uncomfortable with such raw feeling.  It takes someone who’s been there or — better yet — who’s there right now.

Moreover, you get about thirty days of undiluted sympathy from the non-bereft.  Then you’re expected to make efforts to return to regular life.  Even quite good friends are capable of asking, “So, how are you now?” or, “How are you doing these days?” or, “Any plans to get away for a while this summer?” They also make every effort to avoid mentioning the person who has died. His or her name simply disappears from what they have to say.  They mean well.  But they just don’t get it.  And they don’t comprehend your inner confusion, if you try to explain it to them:  Are you really missing him (or her) so much as the weeks and months begin to pass?  Or is it the life you built and lived together that you miss?  Nor do they grasp the hot rage that alternates with your despair: The death wasn’t the fault of the disappeared, so why are you so angry, and (for God’s sake) at whom? After a while, you realize it’s futile to reach the uninitiated.

You can talk about all that in a bereavement group.  The others may come from other professions, other social circles, backgrounds, cultures, faiths…may have other vocabularies, may be less able than you to articulate what’s going on with them inside. But they will listen respectfully and with interest to what you need or want to say. They will have felt what you are feeling, or will begin to feel it as you talk about it and they let it well up.  You (and they) are in a place where it’s safe to let it out.

You also learn coping strategies, or work them out for yourself, from listening to those a little further away in time from death than you are. In addition to the good ideas you pick up, you may also on occasion feel privately superior to some of the group participants.  For example: one poor fellow in his fifties whose mother had died several months before said he wandered around the local supermarket in the evenings although he had no need to shop, so as to feel himself among other human beings. Although I felt sorry for him, I knew at once that’s something I simply would not do. And if you’ve come to the meeting with the sense you’ve been crushed by loss, perhaps beyond repair, hearing about such desperate measures may energize you to find a more palatable and self-respecting alternative.

Some people even make new friends from among those who are sharing their experience.  A mini-group of four who participated in one of the two six-week group sessions I attended  last summer banded together for the purpose of not being alone on Saturday nights.  They pick a local movie by e-mail and all have supper at a nearby restaurant before the movie begins. I myself would not find a shared loss sufficient basis for pursuing friendship outside the bereavement group unless there were other interests and points of view in common.  But it seems to give these four considerable comfort, now that they are all without partners, to spend “date night” doing something together that they did with their partners before.

Why do I still occasionally go to bereavement groups now that it’s six and a half months since Bill’s death? Because I’m in no way out of the woods yet.  The rawness of the injury (and death of a partner is a severe injury to the survivor’s sense of self) has scabbed over. But in my case, anyway, the depth of the sorrow seems to have been somewhat deferred, given the fact that I had to spend June, July, August and September winding down Bill’s affairs, getting a condominium townhouse ready for sale, marketing it, looking for an apartment to live in after the sale, coordinating both contracts so that the apartment contract was contingent on the successful sale of the condo, downsizing, working with a contractor to somewhat alter the apartment before the move, and then finally moving.  (Some of that perhaps to be recounted in future posts.) Such concentrated activity left only early mornings and nights for unrestrained crying. So it is just now when I am “settled” again that I have the relative leisure to let myself fully experience how I feel as I embark without him on this new life into which I was thrust against my will.

And for where I am in what could be called the grieving process, a group can continue to be helpful. I’m the sort of person who responds to what someone else has said rather than initiating a train of thought myself.  Last Monday, at a walk-in session, I responded to a widow who told us how she was sorrowfully trying to recreate the Thanksgiving she had had with her husband for so many years — with a thought I hadn’t been able to formulate clearly before she spoke. I said I felt as if the life I had shared with Bill now seems to me like a play in which I was suddenly left onstage without the other player.  But half a year later, I’m not in that play anymore.  The scenery’s been struck and they’ve mounted another play on the stage, with new scenery.  I certainly remember the first play. I know all the lines. And I dearly wish I were still in it with my co-star.  But I’m not.  He’s disappeared. Now I’m the lead character in this new play.  Except I’ve only been given the first few pages of the script and I have no idea at all yet what the author,  whoever the author is  –me? — has in mind.

That’s exactly how I’m feeling this Thanksgiving.  But I don’t think I could have discovered such an apt and clarifying metaphor for it if I hadn’t been at the bereavement group meeting last Monday. I’m sure there will be post comments from people who’ve had other, more negative, experiences with bereavement groups. But as I said at the beginning, and as Bill always said when someone said or did something that flummoxed us, we’re all different.

I wish you a warm and tranquil holiday weekend.

TRUMP AND LIFE

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Yesterday I declared I wouldn’t be commenting on the election. However, I just came across a piece by Adam Gopnik, published four days ago by The New Yorker Digital News Desk, called “Talking to Kids About Trump’s Victory.” Gopnik’s last paragraph strikes me as so exactly right — not only about Trump arriving after eight promising years of Obama but also about life in general, especially as I have been experiencing it recently — that I can’t resist quoting it.

The lesson of history—one of them, anyway—is that there is no one-way arrow in it, that tragedy lurks around every corner, that the iceberg is there even as the mighty Titanic sails out, unsinkable. [italics mine] Having a tragic view of life is compatible with having a positive view of our worldly duties. This is a big and abstract thought to share with children, of course, and perhaps, like so many like it, it is teachable only as a pained—at this moment, acutely pained—daily practice.

Is a quote a comment?  Probably.  Is life really tragic?  If you live long enough, it does seem so.  Must we nevertheless keep a positive outlook on our familiar duties and pleasures, and take as much comfort as we can from them? What other choice is there?

BIG WORD FOR FEELING AWFUL

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[Whatever the headline may suggest, this post is not about last Tuesday’s election.  My feelings about that are indeed awful, as if someone had suddenly and unexpectedly died, except it’s not the heartrending death of a someone but of political, ethical and perhaps even personal life as I and everyone I know has come to expect it. However, everything that can be said at this point has already been said, by other bloggers, columnists, friends.  As for the frighteningly uncertain future, we can only grit our teeth and wait for whatever comes next. So I am returning here to last May, after Bill’s death and my visit to the undertaker.]

Bill died on a Friday. On Saturday morning, of necessity, I visited the undertaker/funeral director. I then got myself home and didn’t go out until Monday.  There were comforting phone calls, which made me sad when they ended because I was alone in the house again. There was also cuddling with the cats and raw sorrow.  It felt as if a large part of me had been cut away, leaving a hollowed-out bleeding cavity. Solicitous acquaintances sent flowers.  I had no desire to eat (although I knew I should), and wished I could sleep (but couldn’t).  The refrigerator was still full of Orgain, a packaged drink somewhat like Ensure but designed by a doctor undergoing treatment for cancer and allegedly composed of more nutritious ingredients, which Bill had been able to consume even when the medication he was taking to slow the progression of his pulmonary fibrosis removed his appetite and made him nauseous.  I survived the first weekend on two or three daily vanilla Orgains.

I did go to bed early and lay there until it was light again, but if I slept (and I probably did, in fitful bits) I don’t remember it. I do remember my law-school-trained mind spinning like a kaleidoscope gone crazy, unable to focus either on my misery or what I had to do next on Bill’s behalf.  Which was to (1a) sell the red Honda he had driven; (1b) try to return to the distributor for credit his newest and virtually unused portable oxygen concentrator,  five pounds lighter than the one Medicare had provided — for which he had paid nearly $2000; (1c) close his credit card accounts; (1d) notify his insurers of his death; and (1e) verify that I would not need to probate the will, since New Jersey doesn’t require it if the decedent owned nothing solely in his own name at the time of death. There was also what had to be done, all by myself, on my own behalf. Which was to (2a) sell the condo as soon as I could, since it was both too big and too expensive for me to maintain alone much past the end of the calendar year without seriously dipping into capital; and also to (2b) find another place for the cats and me to live as soon as the condo was sold, although the money to buy this “other” place, when I found it, was solely the equity in the still unsold condo because I was pretty sure I didn’t qualify for another mortgage while I still had one. (A few weeks later, I found out I was right.  I was coldly informed by loan officers at two separate banks that I would need to show at least $10,000 in monthly income to carry the two mortgages, even for only the three months or so before the condo would presumably sell.  Hah.  That was not something I would ever have been able to do, even when I was working.)

The (1a-1e) through (2a-2b) in the prior paragraph is of course so neatly organized because I am writing this piece six months later; organization or any kind of  plan was completely beyond me that weekend.  My mind lurched from “close his credit card accounts” to “see if I can get a mortgage” to “should I take the car to Honda or try to sell it myself” to “do I know a lawyer I can consult about the will who won’t charge me” to “the condo is an unsightly mess of medical equipment and books all over the floor” to “how could he leave me to deal with all this by myself?” to “I need more Orgain from Amazon, chocolate flavor this time.”  Then one of the cats, still missing Bill, would come to the bed in the middle of the night to be scratched, petted and comforted. And I would cry, in the dark, into her fur.

Everyone who called advised doing nothing for a while until I felt stronger.  That was good advice. But the Type A person I also am thought: What do they know?  “Listen to what your body wants,” said Bill’s niece, a psychotherapist practicing in Israel.  Well, all right.  Unfortunately, by Monday — when I attempted to walk to the brick mailbox stand two driveways away from mine — I realized I could move only very slowly and was wobbling. Was my body trying to tell me something? I began to eat again, carefully, because I knew I should, and also because kind acquaintances were deluging me with offers of meals at their house, meals at restaurants, prepared meals brought in (one even vegan and surprisingly tasty) — none of which I could in good conscience refuse — and also because a survey of the refrigerator and pantry cabinet revealed so much food stored there to tempt Bill’s appetite that I would have to give it away, throw it all out or begin consuming some of it.  Sleep didn’t come as easily as the meals.  And the trips to the mailbox were becoming even more difficult. By the end of the first week, I was making them only every other day.  (Since Bill was the King of Catalogues, that meant the box was so stuffed when I did eventually open it that I hardly had the strength to pry out its contents and scraped the outsides of my fingers raw on the metal sides of the opening.)  A friend who picked me up to feed me rotisserie chicken and salad had stone slabs for steps up the grass from her driveway to the house. I had to ask her to let me clutch her arm to make it to the front door.

This was both embarrassing and worrying.  I was all alone in Princeton.  Although they were warm and supportive on the phone, one son lived in Florida and the other shuttled back and forth by train between work in D.C. and weekends with his still-young children and wife in New York.  If I became too weak to take care of myself, not to mention all the things needing to be done, then what?  By the time I stepped out the door to get the mail a week to the day after Bill had died, my heart was pounding loud and frighteningly fast, I gasped for breath as if I too had suddenly developed pulmonary fibrosis, and I was so dizzy the ground under my feet spun around. As I proceeded very slowly towards the box with legs far apart, like Charlie Chaplin, to keep some kind of shaky balance, I felt I might be on the verge of dying — not that very minute, but soon.  Although my head was still revolving like a top, I was able to grasp and hold on to one thought:  Call a doctor before it was too late.

Easier said than done.  For nine and a half years, since coming to Princeton, Bill and I had been seeing an internist highly recommended by the nurses in the major medical practice nearby as the most patient-friendly.  Dr. L. was indeed apparently much interested in each of his patients, at least for the time allotted him by the insurance companies, and even seemed to remember just about everything about you when you showed up for bi-annual checkups without first having to review your chart in your presence. But as we each grew older, and more symptoms of this and that surfaced, Bill pulled away. He was mostly seeing specialists by then, anyway.  I hung on to Dr. L. until last year, although Bill kept urging me to switch to Dr. G., another internist in the same practice whom he liked much better on the one or two occasions he had consulted him.

The cause of Bill’s disenchantment with Dr. L., and eventually mine, was that patient-friendly as he was, Dr. L. was a worrier. He was also perhaps over-impressed by our academic and professional credentials and shared all his proactive medical hypotheses with us.  If there were a symptom or a complaint, he not only knew all the conditions and diseases of which it might be a harbinger, which would need to be tested for, but would share all this (potentially scary) thinking with us.  In my seventies, I was sufficiently healthy that Dr. L.’s proclivities as one’s medical advisor didn’t really bother me. Later it did, very much. By then I had enough to worry about, without contemplating dire possibilities that might not come to pass.  But that’s another post, for another time.  Suffice it to say that last March, Bill prevailed, I switched to Dr. G., and obtained an appointment for the end of May.

Thus, in the middle of May when I suddenly needed him, Dr. G. had not yet met me. Moreover, a phone call revealed he was completely booked through the end of June, and certainly couldn’t squeeze in a new patient he didn’t yet know.  Although no one suggested it, I felt unable to return to Dr. L.  Nor would I under any circumstances take myself to the Princeton ER, given my recent experiences at that hospital.  (See “After Death, What?” TGOB, July 29, 2016.) However, Dr. G.’s appointment secretary was very kind when she learned my husband had recently died and I felt as if I were going to die too.  Her husband had died two years previously and she had felt exactly the same way.  She would try to find someone else to see me. (I did hope it wasn’t going to be Dr. L. but kept that to myself.) Good as her word, she called back an hour later with the name of Dr. S., who had recently joined the practice and therefore had an opening, five days from then (no, not sooner), at 8 a.m.

Beggars can’t be choosers.  In the meanwhile, I googled Dr. S.  His photo showed pink cheeks, a big smile on a round young face, lots of neatly combed dark hair; he looked as if he’d just emerged from college. Although he hadn’t gone to any of the medical schools known to me through fifteen years of living with Bill (a psychiatrist), young Dr. S. had practiced for a couple of years in Philadelphia, could probably determine whether I was dying or not, and could then hand me over to the appropriate specialist(s) to treat whatever was wrong with me.

Dr. S. looked exactly like his picture.  He might have been a classmate of  one of my sons when in their twenties.  Still, he was an M.D..  I explained why I was there. Husband died ten days ago. Heart fast and pounding. Unable to breathe. Legs like cooked spaghetti.  So dizzy the world was turning round and round.  No balance.  Unable to think a straight thought.  “Well, let’s see,” said young Dr. S. soothingly, reaching for his tools.  My blood pressure was normal.  My heart rate was normal.  My blood oxygenation level was 98-99 (so the breathing was normal).  “Then why am I feeling like this?” I demanded. “As if I were going to die?”  Young Dr. S. must have been a very good student in whichever medical school he had attended.  He knew exactly what ailed me.  It sounded as if it had come right out of a textbook.

“Somatization!” he declared.  

He meant it was all psychosomatic.  The pounding heart, the breathlessness, the vertigo, the loss of balance, the inability to focus.  I had never heard the noun form before, but if there’s a medical adjective, there’s usually a big and latinate related noun. “It’s just a reaction to your loss,” he said to me in a voice appropriate for addressing a small child or someone not quite with it.

And what was I supposed to do with this information? Learn to live with it? Dr. S. mentally turned pages till he reached the one that dealt with treatment for the grieving patient. He then told me I needed sleep and food. I was to get eight hours of sleep, and if I couldn’t fall asleep when I went to bed, I should get up and read till I felt sleepy, and then try again.  I was to eat whatever I wanted, even if it was french fries, without worrying about it, because I now needed the calories.  I suppressed various impulses to tell him I wasn’t stupid and instead listened impassively, not quite the good and grateful patient contemplated by the medical textbook but close enough. What was the point in pushing it with young Dr. S.?  He was doing the best he could.  He also told me to exercise. “Even if I’m moving like Charlie Chaplin, but more slowly?”  Yes, exactly.  And then I would start to feel better.  Well, perhaps that’s what the medical textbook said. “Could you also write a scrip for ten days of a mild sleeping pill?” I asked.  “To get me through till my appointment with Dr. G.”  No, young Dr. S. feared I might become addicted.  If I really couldn’t sleep after the getting up and reading for a while, I might try Benadryl, which is over-the-counter and not (he said) addictive.

While waiting in line at Rite-Aid to pay for the Benadryl, I thought about Dr. S.’s big word for feeling like death.  Somatization. I had never believed that symptoms of what were later diagnosed as real physical complaints, like chronic fatigue syndrome or Lyme Disease, were psychosomatic, even if they were first dismissed as such.  Apparently I was wrong. It seems in some instances the body does speak up to tell you what you’re really feeling.  Mine, for instance. It was saying that all of me was suffering from mortal grief, even where my heart was actually beating regularly and my lungs actually functioning normally. I had just been been in shock too great to realize it.

And that did make me begin to feel better.  Or at least less worried. The Benadryl was a bad idea; one tablet knocked me out for eleven hours and left me woozy for twenty-four.  But after that I began to fall and stay asleep without help, except from the cats.  So although I continued to weep often and spontaneously when by myself, I had become somewhat more optimistic about being able to manage living without Bill, even if unhappily,  by the time my scheduled appointment with Dr. G. rolled round.

The following week, the undertaker called me to come pick up Bill’s ashes. For the $3,000 I had paid him he probably would have kept them for a while, had I asked. But better sooner than later, and be done for good with that unctuous and falsely sympathetic man. The bag containing the plastic urn seemed surprisingly heavy when I picked it up, although Bill hadn’t been tall or big-boned.  Regretfully, I needed Mr. Unctuous to carry it to my car for me.  I hadn’t thought to bring a cane (although there were eight or nine of Bill’s, in various styles, in the house) because I wasn’t used to needing one.  But I was still afraid I might fall if I held the heavy bag while going uncertainly down the incline from the funeral home door to the curb.  However, I wasn’t dizzy anymore, and that was something.  Besides, Dr. G. had written a scrip for physical therapy to get me stronger again and I already had a first appointment scheduled.  He had also given me another prescription, for thirty days of a mild sleeping pill.  I did fill it, but by then I no longer wanted or needed sleep aids. Six months later, the thirty little pills are still in the drawer of my bedside table.

AND THEN…

Standard

I can’t tell you what happened after I drove away from the Princeton hospital in the middle of the afternoon on May 6 because I don’t remember much about it, other than that I kept swerving erratically as I turned the wheel and was repeatedly honked at.  I suppose I survived because the honkers were also good drivers.  But I did manage to get myself back into my own driveway behind Bill’s red Honda, and then into the house through the garage door, carrying the hospital plastic bag containing everything he had had on when we had checked him in seven days before.  I couldn’t unpack it.  I just put it down.  It was all I had left of him.  It would still smell of him.  And I had to save that until I could cry.

Just then I couldn’t cry.  I sat on the family room sofa to call my two sons to tell them it was over.  They must have said the right things, each in his fashion, but I don’t remember what they said.  Did my voice shake? It must have.  I don’t remember.  Then I must have used Bill’s phone, which had a reduced overseas rate plan, to call his oldest niece in Israel and afterwards his Swiss first wife, mother of his older son, in Geneva.  His niece, who is a psychotherapist, was very kind. I do remember the kindness of her voice, but not her words. It was something about now I had to take care of myself.  His first wife (who speaks English and also likes me) was so matter-of-fact that I actually do remember what she said. It was that she was sorry but after all he had lived a long life, and I had my sons. She also invited me to visit if I ever come to Switzerland.

After that, I must have fed the cats and petted them and petted them.  They knew something was wrong.  Bill hadn’t been home for a week and I was clearly not myself.  They kept rubbing their furry cheeks against me in an unusual display of either affection or distress. I cleaned the litter boxes, and forced myself to drink an Orgain, of which there were over a dozen left in the fridge for Bill.  (Orgain is a somewhat more nutritious, and expensive, version of Ensure, that last nutritional resort for people who have difficulty eating enough).  I was numb.  I put my checkbook in my purse for tomorrow and went upstairs with the sole thought that I had to get some sleep because the next morning I needed to drive to the undertaker, who would have by then removed the body from the hospital — to pay him for having done that and for the cremation that would follow.  We had some old sleeping pills in the bathroom cabinet, but I was afraid to take one, or even half of one, lest I not wake up in time.  I stayed in bed all night, but if I slept I don’t remember it.

The undertaker was professionally solicitous. Sleepless and still in a state of shock, I resented it. He didn’t know me, he didn’t care about me, he was really only interested in my business — which he was going to get anyway because he took care of 90% of the dead in Princeton (as he was quick to assure me when I inquired).  I particularly resented his oily deference and lowered voice when, after obtaining the requisite information for the death certificate, and learning that I had no interest in buying any of his pretentious urns, he informed me that the fee for having removed the body and for the cremation would be $3,000, payable before I left.

Does anyone haggle in such circumstances? Did I really have any viable option?  Deciding it might be more prudent to hold on to cash for the time being, I kept the checkbook out of sight and gave him a credit card in payment.  My mother’s identical cremation in Palm Springs, California, sixteen years earlier, had cost slightly over $300.  I asked him what he charged people who couldn’t afford the fee.  He said if they could prove they were being supported by the state, there was a reduced price, which they could pay in installments.  He also said because his establishment was in the center of town and he needed a lot of space in back for mourners to park, his real estate taxes were very high. He was sure an educated, professional woman such as myself would understand.

The educated professional woman who was allegedly myself didn’t understand much at that point, but she did understand that in a money economy, everything costs.  Even dying.  However, she didn’t have time to brood about it.  There were many other things to attend to.  I had to finalize Bill’s affairs. As important, or even more so, I needed to decide what to do about the condo, which was both too big and too expensive for me to maintain by myself past the end of 2016.  The best time to try to sell it was soon, because people with young children who were looking to buy in Princeton wanted to do it in time to register those children in the Princeton public schools before the beginning of the school year.  So if I were going to sell, I had to get it staged and on the market by early July.  But first, I had to get myself back in shape to function.

Easier said than done.  Bill died on a Friday.  By the following Monday, I felt — felt physically, in my nearly 85 year-old body — as if I might be dying too.