Wednesday, April 08, 2009

One Year Later: Remembering

Tomorrow will be April 9, 2009--one year after my mother's death.

For the last several weeks I've been reliving the events of a year ago:

Last year her birthday was on a Wednesday, and while taking her out to lunch, I noticed that she had trouble eating. Two days later at a P.E.O. meeting at my house, her swallowing problems became more apparent.

By the following Monday, her caregivers were worried that she wasn't eating and urged me to take her to her doctor.

I did so that afternoon and was shocked by how much her weight had fallen: from 110 lbs. to somewhere in the 90s. I had expected the doctor to give her an appetite stimulant or do something helpful, but instead she diagnosed my mother's condition as "end-stage dementia" and told me that I needed to place my mother on hospice.

The doctor had urged me to do this more than a year earlier, but I had said I would wait until some health crisis precipitated it.

Now she asked if we wanted to have my mother fed by intubation or not; my siblings and I said no to that kind of feeding. That meant that she would die naturally by starvation and dehydration (the usual cause of death in end-stage dementia). Hospice doesn't usually allow an IV for hydration, and her assisted-living residence does not allow IVs.

Even as I finally began working with hospice, I still expected my mother to live several more months--no one told me how quickly the end could come.

The next three and a half weeks were a whirlwind of get-acquainted meetings with 5-6 people each from two hospices: the initial person with whom one signs up, the nurse in charge, the nurse's aides (various ones on various days), the physical therapist, the social worker for the spiritual well-being of the family, etc. Because the first hospice's aides took her to meals without her false teeth in, I changed to another hospice.

I soon figured out that the hospice services provided as much morphine as we asked, and an hour or two per day of physical care, but no hours of just sitting with the patient. (Actually, in my two experiences with hospice, they seem overeager to provide morphine, almost saying, "Here you go, use as much as you want; just keep her out of pain.")

Meanwhile, the caregiver who worked with her 4 hrs. per day on five days per week made a trip to visit family in the Philippines.

I decided (with my siblings) that Mom needed someone to sit with her around the clock, especially at night, so I contracted with an agency to do that, meeting the owner and several new caregivers who would do various shifts.

It was a nightmare of worry: meeting with all these people, trying to get my mother to eat and take her medicines, making calls to Bill and Jim and Emily to discuss these issues and advise my brothers to come for last visits.

But my mother was losing the ability to swallow. We gave up on soft foods and turned to pureed foods, then to Ensure only, then to water. And finally she could not swallow water.

A year later I remember two moments in particular out of all this whirlwind.

1) A kind RN, Jewish, who in her initial assessment visit with my mother said, "Oh the poor dear, she's so weak. She's dying. Yes, she will not last more than a few weeks."

She said this maybe 10 days before Mom died. It was so helpful to have someone speak directly like this--it changed my approach. A few days later I stopped trying to get my mother to take her pills.

2) The other moment came on the last Saturday afternoon of my mother's life. My sister had visited her in the morning, and I was going to spend the afternoon with her, looking forward to an intimate time of talking and sharing with her, perhaps reading a psalm or praying with her.

I wanted to drive her somewhere to see the poppies blooming or see the ocean from the Santa Monica pier. We did go to the pier but she was not too interested.

Back at her room, I settled down for a quiet time with my mother, but the evening caregiver came an hour early. I remember being disappointed but not having the courage to tell the caregiver to leave.

Instead I went home, went to dinner with my husband, and came back at 10 pm to spend the night on the floor of the room when the caregiver had to leave. She was asleep when I arrived and did not wake up more than once briefly in the night while her Depends were being changed. I spoke to her briefly then.

I wish I had taken the time to clear out all the caregivers and other concerns in my life and just spend several quiet hours with my mother... but I didn't realize she had only Sunday, Monday, and Tuesday left to live.

In the morning when she woke up, she said, "Anne, are you there?"
"Yes," I said. I got her up, dressed her, tried to get her to drink Ensure or at least water, then took her to church for her last time--a feat in itself.

Then we went to my house, but she was tired, so we returned to her residence. It was all busy time, not face-to-face communication time.

Even on Tuesday evening, her last full day, I taught my class as usual in the morning, returned to Santa Monica, and did not spend more than two hours with her. Even that was with others in the room, discussing care issues: how much morphine she should be getting, how to moisten her mouth, whether she should have a shower or not. I thought she'd live several more days.

I helped her move from her chair to her bed, turned on the CD player with songs like "The Old Rugged Cross," kissed her goodnight, and left her with the caregiver.

The next morning just after 8 am, while I was jogging on the beach, I got the call: "She's having labored breathing."

That started the last whirlwind of actions (call Emily, call brothers, get updates and make decisions with the staff). Emily arrived.

By 10 am, she died.

And then a new flood of decisions and actions had to take place, dealing with the mortuary and the church where her service was to be held. My sister did most of the arrangements with the church; we went to the mortuary together where an inept official made the process much worse than it needed to be.

I don't know why all these events and worries are so vivid a year later.

As it turns out, I am in northern Denmark for the first time in my life, looking up the roots of my Danish grandmother (my father's mother), visiting Copenhagen, Aalborg, Viking museums, old churches with my husband.

But still my thoughts are with my mother one year ago.


Rev Emily said...

see my comments after the birthday post--they really fit more here

Anne Eggebroten said...

Thanks, Emily. Beautiful.

Byron B said...

Thanks for your account of these final days with your Mother. I'm on the same path with mine, and though her final days are somewhere farther in the future, the end will be much like what you have described.

Anne Eggebroten said...

Thanks for your comment, Byron. Yes, for those who have no other serious illness, just dementia, the end is what doctors call "end-stage dementia." Basically your brain can't get your throat muscles to swallow. The person can't swallow food well at first, then can't swallow thick liquids like Ensure, then can't even swallow water.

The family's choices are to have a feeding tube put in the stomach or to watch their loved one decline and starve (also lack fluids). It's very sad to watch (and frustrating--I kept telling my mother to eat, swallow this or that) but it is not that uncomfortable for the person him or herself.

Patt said...

I found your blog while looking for Calmoseptine. That blog made me laugh -- and then I read on. My Mother died last week at the age of 89. I was her primary caregiver -- my brother and sister lived too far away (my sister lives in Boulder, coincidentally). Everything you wrote was so similar to my experiences. My Mom, though, shut her mouth tightly and refused food and died 7 days later. It was very fast and she was not communicative the last 5 days or so which made me sad as I had things to say (although I said them anyway but there was no response)Like your Mom, mine decided also that 90 was just too old and didn't want to go there. Our Hospice workers were angels.
I was so stressed over her care and now I have a freedom I didn't have before -- but I am really scared about the empty spaces in my life. I've stayed busy until today when my sister left and now the tears are coming.
I was just about to start a blog like yours but never even got to the first post before Mom decided it was time to go. I loved her so much and will miss her but am happy for her to be at peace. Thank you so much for your blog. It has helped a lot.