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Maman

Paul Gross


At a recent religious service I attended with Maman, my 87-year-old mother, I watched her fumbling attempts to find hymn number 123, "Spirit of Life," in the hymnal. I held my book up, opened to the appropriate page, so that we both could sing from it.

She glanced up momentarily, tightened her lips, hunched forward and resumed turning pages, finally arriving at the song when the congregation was singing the second verse, which she needed help finding--what with her poor vision and the swirl of notes and words on the page.

As this ritual repeated itself, hymn after hymn, it occurred to me how much cozier it would be if my mother and I could share from the same hymnal.

It also struck to me how unlike Maman that would be. Her need to do things independently--and the improbability of Maman reciting from someone else's page--capture in a nutshell the difficulties we've experienced with her aging process.

Maman was born in Belgium in 1922. She lived through the Nazi occupation before coming to the U.S. Of her five siblings, only one sister remains.

My father died seven years ago after a lengthy battle with prostate cancer. His death left Maman alone, isolated and without her prime purpose in life--caring for, cajoling and trying to exert her will over my dad. He played the immovable object to her irresistible force. Without another person upon whom to focus her indomitable spirit, she seemed to lose energy. And showed increasing signs of forgetfulness.

A couple of years later, Maman had an explosive falling out with her closest friend in the world, her remaining sister, in a Walmart in Florida. They've rarely spoken since.

She started getting lost en route to our house. Eventually, after a traffic accident, she mercifully gave up driving--without ever acknowledging a reason.

As she started to slide, we pleaded with her to plan ahead. "I'll cross that bridge when I get to it," she said. Then, one day, there she was, on the bridge, swaying above the chasm.

She lost her wallet on a bus, but couldn't remember what bus it was, why she was on it, or even that she'd been on a bus--and then lost the piece of paper with the phone number of the good Samaritan who'd found her wallet.

While out walking, she fell on the sidewalk and broke her nose.

She'd call my brother Eric--an internist with a large geriatric practice--weeping. "I'm lonely." The next day she'd insist that she wasn't lonely at all, that she couldn't remember calling him and that she was never bored and "happy as an angel."

Her circle of acquaintances shrank: A neighbor who'd occasionally stop by. Her building doormen. And, most critically, Sandy--"Poochi!"--an outgoing miniature Chihuahua that Eric gave her.

Through all this she responded with outbursts to any attempts at discussion.

"I'm not lonely! You think I'm crazy! You want to lock me away! If you do I'll throw myself from the roof!"

On my family's weekly visits, I'd survey her refrigerator.

"There's no food here," I'd say.

"That's all right," she'd answer. "I can go out any time I want."

"What did you have for lunch?" I'd ask.

"Oh, I don't know," she'd answer dismissively.

The irony--two physicians with a mother who was living alone, poorly nourished, with no memory to speak of (who knew if she was taking her pills?) and at high risk of falling--was not lost on Eric and me. And yet we wavered in the face of her fierce will, electing to wait until some disaster--a broken hip, a stroke, an accident crossing the street--suddenly and irrevocably changed the equation.

But something else happened. The tectonic plates continued to shift, further eroding her memory and her fight.

During a recent month-long stay with Eric upstate, he tried to interest her in an assisted care facility, with predictable results. But then, eyeing her diminishing faculties, he also refused to take her home.

And we held our breaths.

The furious assault she might have launched a year ago never happened. It was as if her army's tanks had rusted, the soldiers were tired and, most critically, the generals were too distracted to care that there was a war on.

Maman is now staying with us for the month of November. In December she'll return to Eric's house. She is sleeping on our ground-floor living-room sofa, having tumbled down our stairs a year ago. "But I never fall," she says, when we discuss the stairs with her.

Our daughters' former caregiver Marie is now back, looking after Maman several hours a day. Even as they go out for walks or sit on the couch watching a Fred Astaire-Ginger Rogers movie, Maman thinks Marie is only here to tidy up the house.

Much of the time she's typically hyper-cheerful, laughing at Sandy's antics ("Come on, Poochi!"), her blue eyes bright and a little blank, her blonde hair now straw-like. She wears the same clothes for days on end. When she smelled of pee one day and I suggested that perhaps Marie could help her with a bath, she glared at me. Later that day, with a tight grip on the railing, she inched up the stairs--alone and muttering--to bathe.

In the evening she becomes sad and disoriented. I've come upon her sobbing.

"I'm lonely," she says. "I wish I could go to sleep and not wake up. I'll take Sandy with me."

At night, I find her emptying out the wrong kitchen cabinet--peanut butter and jam jars on the counter--in a futile search for tea.

"Do you find that you get a little confused in the evening, or that it's harder to remember things?" I ask her.

"No."

As I head upstairs to bed, I hear her poking around the kitchen, removing dirty dishes from the dishwasher, "cleaning" them and putting them away in the cupboard, where we'll find them, still slippery with grease, in the morning.

"Frying pan...frying pan...frying pan..." I hear her whispering.

The ground is constantly giving way on this journey. We now find ourselves on a stable ledge. But what will the next tremor bring? Wandering? Another fall? A more furious outburst?

Given that my brother and I are doctors, it's ironic that the medical profession rarely enters into our discussions. Maybe it's because neither of us thinks that physicians have much to offer at the moment; in fact, we seem to agree that the best we can do medically is to keep Maman out of the grips of a hospital, where she would only get worse.

What ails Maman is beyond tests and medicines. Just like her last bit of retained memory--the one that says, "I don't need any help!"--that won't show up on any scan.

"I'm glad you're here," she says, hugging me one night in our living room. Then confusion flickers across her face. "You're not going home?"

"No, Maman, we're staying here tonight with you."

"Good!"

For now.


About the author:

Paul Gross is a family physician and founding editor of Pulse--voices from the heart of medicine.

Story editor:

Diane Guernsey

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Comments:
November 25, 2009
Beautiful and sad--as life changes and life stays the same-- How kind of you to "stay the night" with your mother. And then some.
Posted By: Kohar Jones
 
November 24, 2009
A beautifully written and moving piece. Finding the right moment, as your brother did, to orchestrate a change in Maman's living arrangements was crucial. Many people do it too soon or too late.
Posted By: Carol Levine
 
November 23, 2009
Very poignant story that brings up the irony of the our powerlessness as physicians in matters of our own family, or in the face of the insurmountable march of aging.
Posted By: Jeff Borkan
 
November 23, 2009
Your story brought back so many memories of the last years of my mother's life. Despite the pain of watching my mom lose herself in the darkness of dementia, I am grateful I was there for her.
Posted By: Ronna L. Edelstein
 
November 22, 2009
This made me smile. Yes it did. For maman is still maman and you and your brother are still her sons. You are doing the best that you can as sons and coming up against the frustration of the limits of your physicianness (for want of a better word this late at night) Keep going, as sons and families. This journey is not easy but it is always a privilege. One to be honoured and as sacred as the oath you took at graduation. You can't fix maman or her ageing but you can and will make this time with her the best you can. God bless. MAM
Posted By: Muriel Murch
 
November 22, 2009
Thanks for great story, well written. The demands of dealing with Alzheimer's are great and the rewards are few, but you are doing what can't be bought in any care setting, loving the woman despite her frailty.
Posted By: PA Bob
 
November 22, 2009
In the years I directed an Adult Day Health Care program, the staff was devastated many times when we'd realize one of our day patients was not only suffering with physical issues, but was deteriorating mentally. Our Center wasn't equipped to help those who clearly needed increased supervision. We would feel helpless too. The patient was part of our ADHC "family". And then there were the families; they'd ask what they should do. They'd look to our Center for answers! We know that changing the routine and environment furthers confusion. Any solution was filled with worries and imperfections. We know so little, and the feeling of helplessness is hard for us in the helping professions and in our personal lives. The daily stress, the seemingly never-ending attentiveness and repairing of emergencies makes our frailities as caregivers very apparent. Paul, you drew such a clear and heartbreaking picture. We do the best we can and need to be gentle with ourselves. There must be a better way, but we don't know it yet.Love to you and your dear family.
Posted By: Sarita Roy
 
November 22, 2009
beautifully done!
Posted By: les cohen
 
November 22, 2009
As practicing clinicians we sometimes find it most difficult to care for members of our own families, especially aging parents. Like the families of our patients, we find ourselves cast in the role of caretaker instead of healthcare provider. Walking this walk can make us more sensitive to what our patients' families face every day. For an excellent article on meeting the needs of geriatric patients, see Atul Gwande's New Yorker piece, "The Way We Age Now," at http://www.newyorker.com/reporting/2007/04/30/070430fa_fact_gawande
Posted By: Brian T. Maurer
 
November 22, 2009
This is a wonderful story, capturing the vestiges of your mother's life and character as it plays out in this late stage of her life. So many families turn their energies (and often their wrath) to physicians and health systems to cure their parents of the difficulties of aging. You delicately acknowledge the futility of medicine to take care of your mother, and place your energies where they belong - to include her as along as possible in your families and homes. Thank you.
Posted By: Julie Schirmer
 
November 21, 2009
Dear Paul -- My heart breaks as I read your story; all the words and situations capture the blend of pain and love in each moment. A similar situation is happening in my family too. You and your brother are kind sons to have your mother living with you; the downward slide can be so jolting and inexorable. May you have moments of clarity, calm, and closeness through this too. Thank you for sharing your story here. Peace to you.
Posted By: Pam Pappas MD
 
November 21, 2009
Paul, What a lucky woman maman is to have such loving sons and how grounded an understanding you have of your own patients and their families as you treat elderly folk. I wish that in this country we do what they do in Sweden and Denmark. In building apartments they automatically apportion some for young folks, some for the elderly so that there is a mix of ages with the concomitant benefits which each group can offer to the other. I considered myself rich as a thirty year old to have two or three friends who were in their seventies and eighties. I treasured their knowledge, their experience and their memories, and in a small way I was able to assist them with cooking, running errands and keeping them company. Both my grandfathers had died before I was born so knowing two elderly men gave me insights into a world about which I had only read. I hope that maman can see younger folk; especially teenagers. It's amazing what a link they can forge.
Posted By: Janet MacKenzie
 
November 21, 2009
I drove my grandmother to the cemetery recently to visit her parents' graves. The next weekend she told me all about the "sweet little brunette girl" who drove her to see her folks. Yes, it's true--Dementia really is the cruelest diagnosis of all.
Posted By: Stacy
 
November 21, 2009
I was moved to tears by your story. Both of my parents are a little younger than your Maman, early and mid 80s, and totally sharp, but I find myself holding my breath often waiting for the next phase, 85 and older. Thank you for your honesty in writing!
Posted By: Laura Fry
 
November 21, 2009
I find your struggle to be what my husband and I lived through with both sets of parents. And, it does not get easier. The most frustrating part of my own story was the the family physician and cardiologist had marginalized my father, offering neither management tools nor anytihing positive once it was clear that the medications were the only route to keeping him alive, albeit lifeless to what he had been. If you can possibly journal your experiences as adult children, you will be far better able to support he children of your own patients. I so appreciate this journey...and am forever grateful I walked my Dad through until his last breath...
Posted By: Susan Mazer
 
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