I survived a three day period this October which marks the anniversaries of the death of two friends and of my first husband. Leaves fall. I move the herbs into the study and it warms up again. My grand-daughter is moving along in ways that can be described as very very close to crawling and pulls herself up to standing, mostly by using the nearest grown-up. Hickox Street has been widened as it turns into St. Francis, maybe in response to a terrible fatal accident last spring. I ate a glazed doughnut, and felt no regrets.
Then the car lights came on in the middle of the night. That really scared me!
Backstory–a recall, an adjustment to the brake lights, failure of that adjustment. Drained battery, engine light icons…trying to put it all together. Until at 2 am the driveway lit up red. I ran out and tried different things. Fortunately, but who knows why, the lights went off and I limped it to the dealer next day.
Now it is “fixed.” How many times have I tried to do the right thing, only to have it lead to something problematic and unexpected. Outside the laundromat a woman was crying in her green car. I told myself that if she was still crying when I came out I’d check on her. She wasn’t crying by then.
We realized the baby–like many of her relatives–has a bad case of FOMO–fear of missing out. She’ll fight sleep to stay where the action is. I personally don’t really have that any more. Autumn comes to me no matter what I do.
Tag Archives: aging
One Old Lady Watching Another
the old lady
across the way
lives like a monk
I watch her sweep crumbs from the carpet
with a roller
my restless mind
doesn’t stop
I’ve tangled
the skein of black yarn
beyond unraveling
the scissors
regards me with reproach
but I pick it up—
a dark bird
tumbles
through falling snow
Photographs by Isabel Winson-Sagan
Measuring a Lifetime by Janice Willard
Measuring a Lifetime
When I visited my parents at the Hallmark Senior Living Center they appeared suspiciously conspiratorial. They giggled together on a sofa, secretly sharing the mail as though it were a spicy French postcard. He pointed excitedly to an image on a color brochure.
“There, that one! I love the flowing curls.” Her small head delicately balanced on frail shoulders instinctively responded with a dismissive shrug. He took her hand and smiled.
He was not the kind of man who ogled women, but he always noticed their hair. One of his earliest depression era memories was collecting a quarter from neighbors who came for a shave, hair cut or perm from his parents who proudly displayed their barbering licenses on the living room wall.
He told me last week that he didn’t know what to think of all Mother’s abrupt changes in mood and attire. She was always a conservative dresser but now she relished layering her arms and neck with gaudy jewelry she got from neighbor’s apartment sales. She insisted on wearing flamboyant decorative headgear. Some days it was a frilly hat or a boa scarf, but mostly she found lots of headbands and managed to weave them through her hair. He was bothered by the chaotic look of it. I told him maybe she wanted to secure her brain, hold it together, keep it safe from the insidious forces she didn’t understand and couldn’t control.
She suddenly spoke as she turned a page. “Here’s the one for me, the June Cleaver, but in brown with just a light splash of graying around the sides.” I tried to envision her wearing a multi colored Cher mane or a pert Audrey Hepburn brown bob. Her blue tinted white locks were all I’d ever known.
She couldn’t remember how to style her own hair, a simple ritual slowly erased from her memory blackboard. He felt shame not being able to afford help with her personal care.
He read out loud the directions for ordering the $29.98 lifetime guaranteed, professionally styled Hairpiece of the Stars.
“Measure the head from the crown around and from the top to bottom, recording both diameter and circumference.” After sharing a confused look, she slowly got out a faded yellow measuring tape from a woven sewing basket under a chair. This was once her grandmother’s, the same one she used to create perfectly identical dresses every Easter for her four daughters.
They began to measure around her head, then top to bottom. They were both mathematically challenged with limited education. Fading eyesight and diminished memory made it extremely difficult to handle the limp, cloth tape.
After many frustrating attempts, they dropped the brochure and gaily began to measure each other’s heads and necks, arms and backs, and even their faces and smiles. I watched them play, entwined with golden streams of a shared lifetime, dancing a rhythm of careless laughter. A spontaneous yellow swirl measured each precious moment because that was what they had.
Another installment in the Great Mama Saga by Devon Miller-Duggan
Another installment in the Great Mama Saga.
I have a friend who has recently published a graceful and grace-full memoir of her mother’s descent into Alzheimer’s. It’s doing quite well. It seems to me that every other day I see a new memoir of someone or others’ blessed and affirming time with a dying parent. I’m beginning to think that I’m a monster.
In any event, the whole process of living with my mother’s shift into dementia is not graceful, or blessed, or anything but dreadful. It has uncovered or dramatically emphasized parts of her personality that were always there, but that I was always able to keep in a shoebox way under my mental bed. The dominance of her passive aggressive (think Southern Princess, or Titanium Magnolia—though she HATES to be reminded that she’s southern) side leaves me unable to trust any expression of either gratitude or affection from her because it is so clear that, no matter how much true and profound love she has for me, her every action these days is geared to make sure I don’t repeat the Awful Experiment with Assisted Living.
Her increasing inability to manage or handle her own life eats hours and hours of time and life when I could be writing or playing with a grandchild, and I am perpetually tired, terrified that I am going to come down with some typically female-dominant form of heart disease, and stumbling along in a haze of guilt and frustration. And all too often living in a house that smells like it’s on fire because she’s tried again to make toast in the microwave and then pretended that she couldn’t possibly have done the thing that left the blackened lump of bread in the sink…
She believes that she can still travel by herself and that it is some malice of mine that I won’t cooperate with this (she can’t walk unaided, can’t consistently dress or safely bathe herself, and wants me to put her on a train to Rhode Island so she can go hang out on Cape Cod with Former/Current Boyfriend #1, who’s in a nursing home. Where she thinks she’d stay, or how she thinks she’d get back and forth from there to the nursing home, I do not know, but she’s sure she could manage it and I’m just being mean). She keeps wanting Former BF #2 to “come up for the weekend” in spite of the fact that she loathes his obsession with thrifting, is 4 years older than she is, and has a pretty serious heart condition. She sees no reason he shouldn’t drive 2 hours and spend a weekend taking her and her walker out for every meal and to concerts. She claims that I’m the only one who thinks she’s “this crazy.” And I feel both full of whip-smart bravado and misery when I reply to this assertion by asking who knows her best. I don’t remind her of how often she brings me her television
remote and asks me to figure out why she can’t dial her sister’s phone number on it.
She believes she has to thank me at least 3 times for things like heating up her soup or picking up groceries, and that she has to apologize grovelingly for any expression of frustration or anger because she doesn’t trust me any more than I trust her. And she’s right not to trust me. I put her in a place she heartily loathed (to which she consented multiple times on multiple lucid days) because I was so exhausted by seeing her through 3 successive life-threatening infectionsin 6 months that I thought I might simply die myself. I betrayed her profoundly, betrayed our contract that she would live in her tiny apartment on the ground level of our house until she died. And I betrayed her even more profoundly by withdrawing myself from her, by recoiling from the savagery of her response to the Assisted Living facility, and by running smack into an even deeper and more complex entanglement within our emotional lives than I had realized existed.
Every step of my adulthood has been marked by another degree of separation from her, but we’ve managed to keep going in spite of my fighting for my own boundaries and her finding ways to “survive” my latest fence-building, so this should not have been the shock that it has been.
Current wisdom seems to suggest that I should be spending time forgiving and understanding, that I am supposed to be finding some sort of holiness or blessing in going through this stage in our lives, that I am supposed to find some worth in it.
There is no worth in having conversation #1,000 about Boyfriend #2 and why he can’t come up. There is nothing to be gained from watching her hurt and frustration at, having won her battle to come home, finding herself living with a daughter and son-in-law who have nothing left to give her beyond mechanical affection, occasional attention, and careful management of her care by others.
And I am exhausted by the mixture of love, longing, and laughably obvious efforts at manipulation that constitute our relationship these days.
This could go on for years. Her heart is goofily strong. Though the scarring left on her brain by 50 years of MS is, at this stage, both contributing to and inseparable from the dementia, the fact is that, at 80, she can still sort of walk and mostly talk, which is nearly miraculous. She takes no meds other than Vitamin D, which hardly counts. We took a shot at Aricept, but it made no difference. We are where we are and we have no idea how long we will be here.
My ferociously acute elder daughter fusses gently about how I should just not engage in any number of these conversations with my mother. She’s right, but the fact is that I have decades of conditioning to fight on that one. My therapist and I talk about how I need to un-attach myself from wanting things to be different. She’s right, too, but the whole lovely un-attachment thing is awfully foreign to my nature. I’m doing what I can. I take an anti-anxiety med that lets me sleep, spend as much time as I can holding my sleeping baby granddaughter and playing with my grandson. I take walks—though not often enough. I am eating more fruits and vegetables than I ever have and taking a big-gun (to me, anyway) injectable med for my Type 2 diabetes. My doctor found me a new iteration of my anti-depressant that is still under patent so that I’ve been able to move away from the generics that were very much not working. I need to find a new yoga class or a Tai-Chi class, or some class that is proven to help people in my age group keep going, and more to the point, not fall down. I need a month with no one needing anything from me. I don’t actually need a lot that I don’t have, and I’m very aware that my situation is, in many ways, not nearly as bad as it could be.
***
Since I started this blog entry two weeks ago, her birthday has come and gone. She’s 81 now. On her birthday, I took her and her aide and her best friend out for lunch. The day after, my husband, elder daughter, grandkids and I took her to the fancy restaurant at Longwood Gardens and for a st(roll) among the at-their-peak tulips. It was an exhausting afternoon (a 13-month old, a 4-year old, and an 81-year old roll into a garden…it almost sounds like the opening line of a joke), but lovely afternoon. After lavishly thanking us for it as we pulled out of the parking lot, she was mostly quiet—enjoying the gorgeous flowering trees as we drove the back roads. But at one point on the trip, and then again when we got home, she tried to explain to me that she didn’t know where she was. I was confused, since my attempts to explain geographically didn’t seem to help either time. She was clearly distressed. But her evening aide arrived, so I hugged her and went upstairs to curl up with a book and decompress. She came up a bit later to find me to assure me that she’d be “better tomorrow.” I just said, more or less reassuringly, that I knew she would.
It wasn’t until much later in the evening that it dawned on me that what she meant by saying that she didn’t understand where she was had nothing to do with geography. It had entirely to do with her sense of losing herself. Then I understood that when she’d come upstairs to tell me she’d be better tomorrow,
she was trying to comfort and reassure me—that on some level her very frustrating insistances that she can still handle herself are not just her fighting to keep getting to do things she wants to be able to do, but that she is also trying to convince me that she needs less care from me.
That she is still trying to take care of me, and is every bit as caught in the tangle of our relationship as I am, as helpless as I am, as hurt/hurting as I am. More, in some ways—she does not have the kind of emotional support I do (she has avoided therapy staunchly for decades, always claiming that she had nothing to learn from it), and she is, in reality, in brute fact, in nightmare truth, losing herself. I may or may not be the monster in the piece (depending on the time of day or on whether BF#2 has come into the conversation again), but her life is inhabited by a monster, and she is watching/feeling it eat her mind by inches.
It’s not like I haven’t known this. It’s not like I haven’t been aware that there was plenty of justice to her sense of betrayal by me. It’s not like I haven’t worked to keep these understandings close to the front of my brain. What I hadn’t understood (Lord, I can be slow…) was that there were ways in which she is/was still trying to take care of me.
If I believed in a God who made human sense—you know, the one so many religious people like to talk about having a Reason for Everything That Happens—I’d be asking right about now how many times her heart and my heart have to break before this is over. I’d be really grateful to have a list so I could check off the times and have some idea when this would stop.
Devon Miller-Duggan on Her Mother’s Decline: She’s just going. And every time she makes the “crazy” gesture, I want to scream, or punch something hard, or run away, or vomit until I can’t breathe. I want to find some way to pull the spike out of my heart, because that’s what that gesture feels like.
Every day now my mother comes (shuffling hesitantly) upstairs from her ground-level apartment to my study on the top of our 4-level split to tell me that her brain isn’t working. This involves some form of her hands spinning at the side of her head in the nearly universal sign for “crazy.” She’s not crazy, but she’s not okay.
For years now I’ve been trying to get her to just call me on her cell when she needs me or needs to talk to me. I guess that the fact that she couldn’t remember to do that 3 years ago was one of the early warning signs of what was going on in her brain. But she has 40+ years of skills around pretending that she doesn’t have MS, and she masked the decline. Sort of. Or we just didn’t want to see—more likely.
When she moved in with us 11 years ago, her new neurologist told her that the scarring visible on her MRI was severe enough that she shouldn’t have been able to walk or talk. At that point she was still doing both with only slight wobbles, as well as driving safely. So she has a history of over-riding her disease. And we all coasted along pretty well until about a year ago, when words started to disappear from her head with great frequency, and she started bumping the other cars in the driveway.
So, okay. I convinced her to surrender her license fairly easily by reminding her that her driving was putting other people’s great grandsons at risk (her g-g-son is the core and light of her life). And my husband simply started counting up her points for her in their daily Rummy game. We all talked about the changes we were watching and started being a bit more vigilant. But there was still some denial—at least on my part. My husband and my daughters seemed to be more aware than I was—or more willing to acknowledge what was going on.
Then, this spring, she got pneumonia that went septic (spread to the bloodstream). At 97 lbs, she doesn’t have much to fight off an infection with, but she did—mostly, I suspect, because while she was in the hospital with the pneumonia, our elder daughter was in the last stages of her second pregnancy and my mother was NOT going to miss that baby. Then, in post-hospital rehab, she got C-Dif, which is justly notorious for taking out whole wings of nursing homes. But the second of the two antibiotics that will touch it worked, amazingly.
I brought her home mid-way through the C-Dif in order to lower the risk of another opportunistic infection finding a home in her teeny self, and we had visiting nurses until she was clear. Now we have a couple of hours a day of in-home help—it makes a huge difference to have someone coming in the mornings most days of the week to do breakfast and a walk and maybe a drive to look at scenery. All this is now necessary because, although she gutted through two killer infections, my mother did not come home with her brain intact. The dementia that had been creeping up on her already scarred brain got a serious foothold while she was sick. She came home confused and needy and sad.
But we got settled into the new routine. Into the “new normal”—a phrase I have always hated, but have come to appreciate in the past 6 months. And we needed a break. So we took her back to the nursing home (not in the nursing ward) for a week of respite care, and headed off to Maine, where we ate a lot of lobster and a great many blueberries, slept, took long walks, and just generally rested our brains and spirits.
I’m pretty sure that nothing went wrong at the nursing home—both daughters were there several times during the week, as well as our lovely rector. But mid-week, her cognition took another tectonic slip. The nursing home checked for a UTI (a perpetual problem for late-stage MS patients), but no medical reason presented itself. When we got home I took her to see her doctor, who offered to do bloodtests in an “if that would make you feel any better…” voice. We exchanged a long look and I declined.
She’s just going. And every time she makes the “crazy” gesture, I want to scream, or punch something hard, or run away, or vomit until I can’t breathe. I want to find some way to pull the spike out of my heart, because that’s what that gesture feels like.
I thought it was just me, but my younger daughter carefully asked me the other day whether it was weird that that gesture makes her feel so wildly, desperately sad and angry.
This morning I (gently, very gently) asked my mother what she wanted she wanted me to do in response to that announcement. She said she just wants me to understand.
I am nearly 60 years old. My mother is 80. I was an only child who grew up in the midst of a 23-year marriage that was a battlefield for 22 years. My parents were a pair of starving alpha dogs and I was the last rabbit on the planet. For my mother, I was haven and bliss and weapon and succor and hope. According to her, I am her greatest achievement.
I have spent many years in therapy learning to make boundaries around myself—learning to be separate from my mother. She has gently-but-implacably fought me for every inch of psychic territory. And I learned, eventually, to make and maintain those boundaries in a variety of ways that did not require her
consent or participation. It has not always been pretty, but it’s worked, even with her living in my house. Nonetheless, we are maybe a little extra entwined, interlaced, woven, knotted. Clotted, infested, enmeshed, fused.
I’d really love to say something profound and enlightening here, but the truth is that there is nothing enlightening to say about this. And the situation itself is so profound that it certainly doesn’t need any analysis from me. And I don’t really want any insights now; I just want this to effing stop because I couldn’t possibly scream/cry/vomit/punch my way to the bottom of what it feels like when she tells me that she can’t remember what comes after taking off your shirt, or what you do when someone hands you your dinner, or when it becomes clear to everyone in the room that she can’t remember her 3-month old great-grand-daughter’s name. Or when she can’t remember her 3-year old great-grandson’s name. Or when she makes that gesture. I wonder how many times I can die, how many times my heart can shred or shatter before she’s gone. I wonder how I can bear the simple, brutal facts of not being able to do anything, and of not being able to know anything. I wonder these things every day even as I am deeply aware of and grateful for my exceptional family support, godsend of a therapist, and blessed church community. There’s money enough for whatever needs to happen, I think, provided that things don’t go on too long. All of that helps. But only up to a point.
I am not conflicted in the sense of switching back and forth between two strong, but partial emotions. At any given point in the day I am 100% frantic about who I’ll be when my mother leaves the planet and desperate to have her be better, and 100% hoping that the next time I go check on her, she’s gone, and 100% lividly angry that I am having to handle/manage/experience this, and 100% just bloody sad. It feels a little like having your head filled with Genghis Khan’s entire galloping, sword-swinging army all the time.
The only thing worse would be if I thought I was special. At any given point, there are hundreds of thousands of us walking around with this particular razor-filled stew of anguish and anger and grief and horror and love in our heads. It’s amazing that the earth doesn’t just crack apart.
Whatever faults my mother has, my whining exhaustion should not be her elegy by Devon Miller-Duggan
Last week’s assignment in my Intro Poetry Writing class was an elaborately phrased prompt for an elegy (I cannot recommend the prompts in Challenges for the Delusional from Jane St. Press highly enough. I only use a couple of them in the course of the semester because the real reason I have my students buy the book is so that they can take the marvelous thing away from the class with them…). I don’t normally write with my students, which is kind of dumb. Or it’s a reality-based function of the kind of energies involved in teaching. Or, or, or… But I decided that the elegy was timely, at the very least, given that last week my mother came home from the rehab following her back-to-back life-threatening infections (septic pneumonia and c-dif). I’ve been doing a LOT of processing, emotionally since she was ambulanced into the hospital with the pneumonia 6 weeks ago.
Short background: my mother was diagnosed with MS and epilepsy 3 months after the birth of my (developmentally disabled) sister when I was 15. She’s 80 now and in remarkable shape (she was still driving more or less safely until a year ago). I have no other siblings. Except for the year she ran off to California with a couple of grifters (I swear.) in an interesting attempt to “not be a burden” to me, there hasn’t really be a year in which I didn’t spend some time taking care of my mother, even though she has been largely independent for most of it. She’s lived with us full time for the past 11 years.
There aren’t a lot of 80-year old MS patients out there, and the ones there are are in much worse shape than my mother. Which does not mean she’s in terrific shape. She’s frail, has really lousy balance, truly terrifying toenails, no appetite, and a pretty bad attitude. Her speech is impaired, but mostly functional. Her brain’s been sliding away really noticeably for a year now. Hearing’s iffy and interestingly selective. But she’s on no meds and her heart’s strong.
Here’s the thing. I am the core and focus of my mother’s life. Always have been. According to her, every major decision she’s ever made has been made in the context of me. Every. She stayed with my (toxic to/with/around her) father for me. She divorced my father for me. She took up with her long-time incompetent alcoholic boyfriend for me. She stayed with him for me. She moved with him to Cape Cod for me. She had my (sister against all medical logic because she believed she’d have another me. She moved into my house because I wanted her to (nothing to do with the fact that the aforementioned boyfriend drained her finances to the point where she couldn’t keep her house on the Cape…). I am her greatest accomplishment. Otherwise, according to her, her life is a long list of disappointments. She never got her novel published. Or her diet book. She never wrote her second novel. She never got to take enough classes. She never got to travel enough (several trips to Europe and various National Parks notwithstanding). She never got to marry the Great Love of her life (wouldn’t leave his wife). She never got to have a Ph. D. and teach teachers.
She has never understood that I don’t particularly want to be the focus and core of her life. Not fully. She understands, on some important, but subconscious level, that I can’t be an actual grown-up without some sort of separateness from her. But she doesn’t like it. I’ve spent decades having a semi-comic conversation with her about the definitions of passive-aggression and guilt-mongering. Makes me feel better. Rolls off her like water off a charmingly twinkly duck’s back. I love her to pieces, but not quite the way she loves me.
And it’s been a largely highly functional relationship. She’s, of course, generous to a fault, and funny and smart and tolerant of my occasional bouts of bitchery and bluntness. We have a kind of system that has worked pretty well for a long time.
But the past 6 weeks have just about broken me. The hospital was a nightmare—I stayed the first 4 nights to keep her from getting up and falling on her face repeatedly (the nurses couldn’t get there fast enough, even with a bed alarm—she’s weirdly fast for a wobbly 80-year old—as it was she did rip out her lines once…). The rehab was worse. Good rehab, great care, still the most depressing place I’ve ever been. Now she’s home and I’m functioning as her caregiver until we get all the home-health stuff settled and in place. I’m also teaching and caring several morning a week for our 3-year old grandson (a more joyous human never walked the planet) and trying to spend enough time with my brand new granddaughter (oh, yeah, my daughter was in labor for a week in the midst of all this—but she won and got her VBAC and a gorgeous 9.6 lb. baby). I’m tired in ways I have never been before, and angry with my mother (like she timed this on purpose…) for still being alive, for believing that she needs to stay alive because her love is so magical that it somehow sustains me and all the air around me (that’s not actually a very exaggerated version of things she has said), and for needing me so very, very, very much.
So I’m having a little trouble with the elegy. I’d like it to be about the absolute animal joy of my mother bodysurfing with her granddaughters on a beach on Cape Cod Bay one perfect summer day when the normally mild waves were just energized enough to be perfect for it. I’d like it to be about how, even now, when she looks at trees, she’s trying to figure out whether they’d be good to climb (she was a great tomboy as a kid). I’d like it to be about the ferociousness and generosity of her love for her family. About her playing Rummy with my husband most days and the two of them squabbling like siblings. About how, at Yosemite and Bryce and the North Rim of the Grand Canyon and Acadia and Zion, she thanked us over and over and kept saying “I’m going to remember this for the rest of my life!”
But right now, all I can think about when I wake in the morning is how, no matter what else the day holds or needs, it will be another day of begging her to eat and cleaning up her messes and having her ask me repeatedly “What do I do next?” and telling me—achingly and repeatedly—how very much she loves me. Another day of one knife in the heart after another. Another day of realizing that my love has limits, that it can be worn down, wrung out, drained off, and then telling myself that caring for her body is, right now, enough of whatever ultimately indefinable thing love is. And kind of loathing myself for whining. Whatever faults my mother has, my whining exhaustion should not be her elegy.
Last week’s assignment in my Intro Poetry Writing class was an elaborately phrased prompt for an elegy (I cannot recommend the prompts in Challenges for the Delusional from Jane St. Press highly enough. I only use a couple of them in the course of the semester because the real reason I have my students buy the book is so that they can take the marvelous thing away from the class with them…). I don’t normally write with my students, which is kind of dumb. Or it’s a reality-based function of the kind of energies involved in teaching. Or, or, or… But I decided that the elegy was timely, at the very least, given that last week my mother came home from the rehab following her back-to-back life-threatening infections (septic pneumonia and c-dif). I’ve been doing a LOT of processing, emotionally since she was ambulanced into the hospital with the pneumonia 6 weeks ago.
Short background: my mother was diagnosed with MS and epilepsy 3 months after the birth of my (developmentally disabled) sister when I was 15. She’s 80 now and in remarkable shape (she was still driving more or less safely until a year ago). I have no other siblings. Except for the year she ran off to California with a couple of grifters (I swear.) in an interesting attempt to “not be a burden” to me, there hasn’t really be a year in which I didn’t spend some time taking care of my mother, even though she has been largely independent for most of it. She’s lived with us full time for the past 11 years.
There aren’t a lot of 80-year old MS patients out there, and the ones there are are in much worse shape than my mother. Which does not mean she’s in terrific shape. She’s frail, has really lousy balance, truly terrifying toenails, no appetite, and a pretty bad attitude. Her speech is impaired, but mostly functional. Her brain’s been sliding away really noticeably for a year now. Hearing’s iffy and interestingly selective. But she’s on no meds and her heart’s strong.
Here’s the thing. I am the core and focus of my mother’s life. Always have been. According to her, every major decision she’s ever made has been made in the context of me. Every. She stayed with my (toxic to/with/around her) father for me. She divorced my father for me. She took up with her long-time incompetent alcoholic boyfriend for me. She stayed with him for me. She moved with him to Cape Cod for me. She had my (sister against all medical logic because she believed she’d have another me. She moved into my house because I wanted her to (nothing to do with the fact that the aforementioned boyfriend drained her finances to the point where she couldn’t keep her house on the Cape…). I am her greatest accomplishment. Otherwise, according to her, her life is a long list of disappointments. She never got her novel published. Or her diet book. She never wrote her second novel. She never got to take enough classes. She never got to travel enough (several trips to Europe and various National Parks notwithstanding). She never got to marry the Great Love of her life (wouldn’t leave his wife). She never got to have a Ph. D. and teach teachers.
She has never understood that I don’t particularly want to be the focus and core of her life. Not fully. She understands, on some important, but subconscious level, that I can’t be an actual grown-up without some sort of separateness from her. But she doesn’t like it. I’ve spent decades having a semi-comic conversation with her about the definitions of passive-aggression and guilt-mongering. Makes me feel better. Rolls off her like water off a charmingly twinkly duck’s back. I love her to pieces, but not quite the way she loves me.
And it’s been a largely highly functional relationship. She’s, of course, generous to a fault, and funny and smart and tolerant of my occasional bouts of bitchery and bluntness. We have a kind of system that has worked pretty well for a long time.
But the past 6 weeks have just about broken me. The hospital was a nightmare—I stayed the first 4 nights to keep her from getting up and falling on her face repeatedly (the nurses couldn’t get there fast enough, even with a bed alarm—she’s weirdly fast for a wobbly 80-year old—as it was she did rip out her lines once…). The rehab was worse. Good rehab, great care, still the most depressing place I’ve ever been. Now she’s home and I’m functioning as her caregiver until we get all the home-health stuff settled and in place. I’m also teaching and caring several morning a week for our 3-year old grandson (a more joyous human never walked the planet) and trying to spend enough time with my brand new granddaughter (oh, yeah, my daughter was in labor for a week in the midst of all this—but she won and got her VBAC and a gorgeous 9.6 lb. baby). I’m tired in ways I have never been before, and angry with my mother (like she timed this on purpose…) for still being alive, for believing that she needs to stay alive because her love is so magical that it somehow sustains me and all the air around me (that’s not actually a very exaggerated version of things she has said), and for needing me so very, very, very much.
So I’m having a little trouble with the elegy. I’d like it to be about the absolute animal joy of my mother bodysurfing with her granddaughters on a beach on Cape Cod Bay one perfect summer day when the normally mild waves were just energized enough to be perfect for it. I’d like it to be about how, even now, when she looks at trees, she’s trying to figure out whether they’d be good to climb (she was a great tomboy as a kid). I’d like it to be about the ferociousness and generosity of her love for her family. About her playing Rummy with my husband most days and the two of them squabbling like siblings. About how, at Yosemite and Bryce and the North Rim of the Grand Canyon and Acadia and Zion, she thanked us over and over and kept saying “I’m going to remember this for the rest of my life!”
But right now, all I can think about when I wake in the morning is how, no matter what else the day holds or needs, it will be another day of begging her to eat and cleaning up her messes and having her ask me repeatedly “What do I do next?” and telling me—achingly and repeatedly—how very much she loves me. Another day of one knife in the heart after another. Another day of realizing that my love has limits, that it can be worn down, wrung out, drained off, and then telling myself that caring for her body is, right now, enough of whatever ultimately indefinable thing love is. And kind of loathing myself for whining. Whatever faults my mother has, my whining exhaustion should not be her elegy.
Not Exactly Resolutions
For many years, a close friend of mine and I have shared life coaching with each other. Recently we decided we needed a ten year plan. Here are some initial questions we answered.
Please feel free to add your thoughts!
What does it mean to be our age? (approximately 60)
What wisdom, creativity, and track record do we have?
What is the source of our energy these days?
Is drive the same?
How can we adapt to a changing inner and outer world?
How much more change is possible? (My wise friend noted that change is infinite and ongoing).
Do things seem more or less limited?
How do we deal with ongoing issues of health and employment in us and our families?
And my favorite–
Is what we need what we want?
I’ll Never Be Hip
Keeping Up With The Times
I had a funny bonding experience this week with the lovely woman who sells me a coffee (weak Americano, extra cream) from her cart. I admired her nails. We agreed we both loved floral things because we came of age in the Seventies. I said I was trying to give up floral prints for say, a more mature look, like stripes. She said–why bother?
I’m turning 57, and I must admit I will never be hip. I wasn’t hip young, and I’m not hip old. Maybe I’ve been too dreamy, living too much inside my head. When my first husband Robert died (now more than sixteen years ago) I found myself sobbing–now I’ll never know what is hip. Robert knew about World Beat before the world did–the strange, obscure, funky, artsy item just seemed to come naturally to his hand. I am so unhip that I still think it is cool to eat sushi.
I’ve led a modestly adventurous life, and found myself in some very unusual places (raising a 3 year old in a Zen monastery, in a living module in an abandoned airforce base in Utah) but I’ve remained pretty 1970’s–I like my clothes soft and flowing, and I can sling the word “patriarchy” around even though by now it is beyond passe.
As I said recently in response to a comment on the Mad Men piece-I’m happy to take advice from those who are au courant.The younger generation told me to watch Boston Legal, Community, Weeds, and now Treme. I like to take a cue from the young (which has led me into all kinds of wild ideological reading). But I don’t try to stay current with media in general as I find it obtrudes too much on my own thinking process.
And I do have a sustained fondness for things of my youth–including floral fabrics and Indian print things.
On Aging by Terry Wilson
AGING
I have 17 different kinds of eye cream—OK, maybe only 13, but more are arriving by mail, any day now. Hydroxatone is supposed to take away the dark circles but after about 4 months of spreading it under my eyes and also on my eyelids that don’t even have circles, I can’t see much difference. I already canceled Dermitage which was being sent to me every month, and none of these potions are cheap! I ordered Cindy Crawford’s Meaningful Beauty because Cindy looks so good and supposedly it’s made from some melon found only in the French countryside, but it did nothing. And when I called to send it back, the representative said that it was too late; the trial period had ended, and now I’m stuck with a lot of Meaningful Beauty.
I have Suzanne Sommers’ Thigh Master to keep my chubby thighs in line, and I have 14 quarts of hair gel, but I’m powerless over my hair and my life has become unmanageable. Aging is basically hopeless, though later tonight I’ll be ordering some Nopalina for the inflammation in my knee. It’s made from the Nopal cactus which survives in the arid Arizona desert—3 ounces a day and your soreness is supposed to disappear. I hope it doesn’t taste bad.
Sometimes I ask my husband how I look before we go out. I’m not always dressed up, but sometimes I am and I say,
“Mark, do I look OK?”
“You look great,” he says, his head in the closet getting his coat. He’s halfway out to the car and I yell after him.
“But you didn’t even glance at me! How do you know how I look?”
“You always look great,” he says, fiddling in his glove compartment. Then his eyes meet mine. “You look fine!”
“Fine?” I say. “What does that mean? Don’t butchers say a cut of ham is fine?”
I see my mother aging and now she has dementia, I hate to say. Still, her skin is as soft as tissue paper, the skin of her face especially, but even on her arms and hands. Once during her 90th birthday party a few yrs. ago, she demonstrated once more how she loves to be the star. I had given her these warm and soft white furry gloves and scarf for those cold Buffalo winters. As we all sat on the couch and opened gifts for her, she put each glove on slowly and then the scarf around her neck. It was November so she was probably cold, and as my sisters and brothers read her these sentimental cards, “I love you Mom; you’re the best Mother anyone could ever have. You’re so kind and loving…” she yelled, “Are you done yet?” And all the while, her hands were in the air, in front of her face as she watched them moving in the white gloves, making wave motions for all to see like she was touching the wind, her hands flying free like Marcel Marceau, expressing her joy at still having hands, still being alive.
Tmwilson222@aol.com
Spirited Sisters: My Self with Gray Hair by Miriam Sagan
When I look in the mirror I see myself…but with gray hair. I see my grandmother who was a worn invalid by mid-life and my mother, who is 84 and teaching high school.
My main feeling about aging is a poignant one–so much time has past, so many things have happened, so many people come and gone. I feel the past with its tidal wave weight of water behind me.
My view is obviously formed by the fact that I haven’t had a healthy body since I was 21. At that time, I had what now, at long remove, appears to have been swine flu. Doctors told my parents I would die. My lungs failed, and I was in the ICU for many weeks (on an oxygen mask before respirators) and for many more in the hospital. I emerged from the Beth Israel Hospital a different person–and one cut over 25% of her torso.
The result was chronic pain, some trouble breathing, and eventually soft tissue trauma and a difficulty walking. The true result, though, was being blasted from one life into another. I became less conventional, I moved to San Francisco, I listened to my own drummer–simply because at 21 I knew, really knew, that I was going to die.
But I can’t remember an intact body. I think aging may be less traumatic for me in that I have truly come to live with limits–vanity doesn’t forbid a cane at 56 that I bought when I was 40. What is more traumatic though is that I’ve got some post stress–including a fear of doctors and a tendency towards self-pity! (what! Another symptom!).
So here I am, looking at 60. Happy to be alive, happy not to have died that ignorant hopeful girl I was. Amazed that I’m already twenty years older than my first husband Robert was when he died. Pleased I can still think of myself as cute as I catch a passing glance.
Teaching is the main thing that keeps me from feeling I’ll get rigid with age. I love the young–their tattoos, pierced noses, purple hair, generational kindness, and yes, hope, in the wake of the world they inherit. I read what they suggest, watch their favorite shows, listen to their music, ask for the techie expertise, and accept their advice.
The best advice I got recently from a 19 year old–“you should just do what you really want to.”
Photo by Hope Atterbury