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Broken promises, love and long nights
Sometime in the last two months, my mother stopped sleeping at night. The hospice nurses called it “sundowning.” My sister-in-law, who had just moved her father into a locked memory care unit, called it “dementia’s 36-hour day.”
Imagine a 100-pound newborn, her days and nights mixed up. Now imagine that the newborn has osteoarthritis and the faint beginnings of pressure sores along her protruding spine and skin the thickness and strength of moistened tissue paper. This is a baby who can neither be swaddled nor soothed.
My mother began pacing the long hours of the night, taking her clothes out of the drawers and piling them on the floor, checking and rechecking for the items she was sure I had stolen. She picked up blankets, looking at them curiously, not understanding where they had come from or whose they were. What she missed, she did not have; what she had, she did not recognize. She was anxious and confused.
“Why are those men here?” I told her there were no men. Later, worn down by her frail mania, I would tell her I didn’t know what the men wanted. Both statements were true.
We hired night caregivers, four kind women working as a team, spelling one another, and spelling me. Three of the caregivers are members of a small holiness church whose ministries include care for the elderly and the ill. One of the caregivers is a nursing student at the local state university. The nursing student is just 19. She is working her way through school.
When the young helper called sobbing one Monday morning at three, I thought she was calling to tell me my mother had died or, perhaps worse, fallen. She called to tell me my mother would not sleep, would not stay in bed or in her chair, would not keep the oxygen tube in her nose. I got up and went through the darkness to where my mother stood riffling through her closet while her helper stood by, crying and saying, “I’m sorry. I’m so sorry. I don’t know what to do.”
Me neither.
I sent the young woman home to get some sleep before her nine o’clock class. I started, again, the story of how I had not taken my mother’s white pants.
I recall a night just after my fourth child was born. She would not sleep, unless I was walking with her or rocking her or feeding her. If I bent to put her down in the bassinet, she startled and began to wail.
I remember watching the clock, knowing how soon my other three children would be awake and ready to be fed and dressed. At some point my lullabies turned into a single tearful refrain, “Please go to sleep.”
Twenty-seven years ago, I had no idea how manageable that infant and her sorrows would someday seem.
The hospice nurses tried giving my mother a chip of an Ativan tablet at bedtime. Then they added a dollop of an antipsychotic. Then more Ativan. My mother’s hallucinations lifted a bit but still she could not sleep.
One of the holiness ladies brought in her laptop and set it up so that mother could watch a real-time video of an eagle in Iowa sitting on her nest, keeping the eggs beneath her warm and safe. There was no music or narration, just the sounds of the wind and the eagle as she ruffled her feathers to resettle on the nest. Sometimes the eagle and her mate called to one another. I quieted as I watched, but my mother could not stop her pacing to imitate the placid raptor.
All of the caregivers had day jobs. My mother alone, like an infant, could sleep on her schedule, a schedule only her body could recognize as in some way ordered.
We kept looking for a nursing home that did not resemble an electronics superstore, with the residents parked in front of the giant screens that everywhere greeted us, in the lobbies, in the dining rooms, in the lounges, in the game rooms, in the residents’ rooms.
We made a pact, my husband and I. The Golden Rule would be the guide. If either one of us could see putting the other in a place, it stayed on the list.
Well ... the Golden Rule and a hefty amount of cash. Doing unto others as you would have them do unto to you in the assisted-living world is much easier for those who share my mother’s lucky trifecta: Medicare, veteran’s benefits and savings.
Then we found it, a well-lit, quiet complex, with exercise classes, an attentive staff and big windows looking out on the mountains. This place offers restaurant-style dining, lectures, concerts and an indoor saline pool. There are scenic drives, lunches out and shopping days. The televisions are dark and silent, except for special shows when the staff tunes in the recent royal wedding or a weekly “I Love Lucy” fest.
But when Mother was evaluated by a nurse practitioner on staff, the recommendation came back that she should be in the memory care unit. This unit is locked, the door is alarmed, and the windows, though also large and looking out on the mountains, do not open. One woman there goes to the windows each day, looking out on the mountains of Colorado and seeing the prairies of Minnesota. Another man watches the garden for signs of a storm. He shuffles to the door, watching and worrying about the ceramic gnomes, the “little people,” he calls them, who get wet when it rains. Others have returned to that time of infancy when sleep comes suddenly and with authority, claiming most of the hours. Some do not speak at all.
Some are more social and verbal than my mother but the not sleeping at night, the sundowning, the 36-hour day, these they hold in terrible common. The number of staffers increases at night.
On Holy Saturday, when I would have usually been in the kitchen glazing the double chocolate cheesecake and marinating the roast, I helped move my mother out of the home where I had prayed she would live to the end of her days.
“Please, take me home,” she begs each time I visit her. “Please,” she cries. “I won’t be in your way. I’ll do whatever you say. I promise. Please, oh, please, let me go home.”
I wish I could pretend she means heaven when she says home but she means my house, where I did, indeed, tell her she could live out her days. I made a promise, and I broke it. How many other times, she must wonder, have I lied?
My cousin went to visit her. She says Mother thought she was Dorothy Jo, a childhood friend, now long dead. Mother told “Dorothy Jo” why she had been forbidden to play with her. It’s because Dorothy Jo’s mother was having a, a -- she stops, searching for the word -- “a, a, a, you know, a screwball with the doctor.”
My mother says, “I know you hated me.” My cousin hugs her and says, “Betty, I love you. And I forgive you.”
Sometimes my mother’s grief turns to anger. “Aren’t you sorry?” she demands of me. “Aren’t you sorry you don’t have me?”
“Yes,” I tell her, weeping. “Yes, I am. I am so sorry.”
Perhaps one of these days, on one of these visits, my mother will be Dorothy Jo, an innocent punished for the sins of another. Perhaps then my mother can hug me, and say, “I love you, Melissa. And I forgive you.”
[Melissa Nussbaum is an NCR columnist who lives in Colorado Springs, Colo.]






Dementia is terrible for the
Dementia is terrible for the sufferer and for the caregivers. It's a source of so much confusion for all parties as the sufferer mentally leaves the present and enters a world that only she (perhaps) understands. You have done so much more for your mother than many could or would have done. Although you were not able to keep her at home, you have ensured that she is in a safe, caring home. That is really the most important part of your promise. Prayers for you and your family. If your mother were able, I'm sure she would tell you that she loves you dearly. You have been faithful to her.
May you both find peace and
May you both find peace and acceptance knowing you did the best thing for her, for you, and for your family. I know we finally found that and I am beyond grateful. My prayers are with you all!
I am reminded of visiting my
I am reminded of visiting my Mom at the nursing facility during her last days. I would sit with her and open her mail. I hated having to go through the mundane pile of meaningless pieces day after day. I didn't realize until after she had died that she actually waited for me to visit her to open her mail. She intentionally waited. She actually thought that it was a joy for me to do this for her; so she told my sisters (Don't open my mail...wait for your brother!). I now know that the mail was meaningless to her.
My mother was also thus, with
My mother was also thus, with my father going to see her daily, even twice a day, while my siblings and I lived elsewhere, visiting only occasionally. My father was a saint.
As long as I live, I will
As long as I live, I will never know why some people must endure such prolonged pain and confusion at the end of their lives. I took care of many just like your mother for many years. My care is now largely devoted to the spiritual and religious needs of the sick and dying.
My heart goes out to you and I will hold you and your mother in prayer.
May God bless and protect you and your mother.
H.G. Bishop Timothy (MacLam)
Pilgrim Prayer & Healing Ministries
How painfully sad. My prayers
How painfully sad. My prayers for all of you. I went through something similar with my father. Please know that I care and understand.
Ms. Nussbaum, may I suggest
Ms. Nussbaum, may I suggest (from personal experience) that the promise you made to care for your mother is best kept by doing exactly what you're doing? There came a point at which our father could no longer be cared for by us lay people in a lay (home) setting. It was a wrenching and daunting task, but I don't look back on it with any guilt. We did what we could reasonably do for him for as long as conscionable. I know we're called to do the challenging, but don't you agree that we're not called to do the truly impossible?
My family went through the
My family went through the same process of (desperately) holding on to taking care of Mom at home and finally admitting we could no longer do it. Altzheimer's took away too much of her mind and Sundowners left us too exhausted to care for our homes and our own children.
My prayers and thoughts are with you and your family. After she was in the nursing home, there were moments of real connection with Mom, of love given and received and known by both of us in that moment. Treasures. May you also have them.
promises are made to be
promises are made to be broken.
my thoughts and prayer are
my thoughts and prayer are with you and your mother, Melissa. I think you are acting with great love and care. It is such a difficult time.
Sending you a warm hug.
Barbara
Dear Melissa, and other
Dear Melissa, and other heroic yet drained care-givers. The only sure promise we can make, it seems to me, is to remain faithful and loving. The shape of that fidelity and love is beyond our horizon of knowing the future and its demands. You are birthing your mother into new life, and the labor is long. May you be held gently as you wait in hope. You are in my heart!
Melissa, Having gone through
Melissa, Having gone through this same heartbreak with my own mother, I fully understand your article.
Following a time of home care and Mom wandering in the middle of the night, we too were faced with putting Mom in a dementia unit at a nursing home. She was there for 9 years.
My sister and I were fortunate that she called us by the same pet names she used for us when we were babies. She did not remember anything else but she remember those names.
We lost her 2 years ago and we miss her terribly. Once we learned how to get into her world, we were able to communicate with her on that level. When she passed, well meaning folks mentioned that it must be such a relief for us. It wasn't. I would give anything to walk in that unit and see Mom's childlike smile as she grabbed my hand and kissed it... just one more time.
Thanks for sharing your
Thanks for sharing your experience with us. You and yours are in my prayers. Sundowning is something my son with autism experiences as well, particularly during the winter months. He wants to go to bed when it turns dark, even if dark is 4.00 in the afternoon. His confusion, tears, and agitation are tough on me, yes, but I can't even begin to imagine what it's like for him. That doesn't make it any easier for me, my spouse, or my little guy's brother to handle day in and day out, as you so eloquently share. Thanks for yet another reminder that no one is ever truly alone in such an experience - that there are others who walk a similar road.
I wish you and your mother the peace which passes all understanding. I haven't quite experienced that yet, but have seen glimpses, so I know it's real.
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