This is the featured article in the Winter 2011 Buddhadharma: The Practitioner’s Quarterly. I’d like to thank Shambhala Sun Publications for permission to reprint it. Although I wrote the article from the perspective of a “practical” Buddhist, it’s applicable to people with other spiritual convictions.
If you are not already a caregiver for someone with a chronic or terminal illness, statistics say you will be. It’s estimated that there are at least 45 million family caregivers in the United States and that number will keep rising as people live longer. You should assume that at least once in your life, you will be asked or feel obligated to provide care for someone who can no longer care for him or herself. It may be occasional and for a short period of time, or constant and last for years.
The question asked by millions every day is, “How do I do it?” The question asked by anyone with deep spiritual convictions, is “How do I do it for someone who holds very different beliefs than me?” As a Buddhist caregiver in both hospices and other settings, and whose caregiving population is nearly all non-Buddhist, I’ve often had to ask myself the latter question. And with Buddhists comprising a tiny fraction of the American population, you too may be faced with the same question.
When Needs Conflict With Buddhist Values
We all have a tendency to look at the misery of others and think, if only they would believe as I do, they could lessen their pain. Our beliefs are often in the form of “if only” propositions. The core message is, “If only everyone followed the teachings of (place your favorite teacher here) the world would be a better place.” And by extrapolation, the person you are caring for could be more at ease with their chronic or terminal illness if only (fill in the blank with your favorite life maxim).
From a safe distance, helpful suggestions based on millennium-old principles seem logical and righteous. I know that as a Buddhist, the application of certain principles and beliefs have made my life more meaningful. From a distance, it’s possible to look at the misery of others and feel the certitude of “if only” statements. But what if the person needing care is your non-Buddhist partner, brother, mother, father, child, or close friend whose idea of “letting go” is trading in a car every two years for a new one. Or “living in the present” means keeping up with current fashion? The objectivity that is possible from a distance dissolves when it’s someone whose hand you can hold. And the universal truth of some concepts, such as letting go and living in the present, becomes equivocal. There is a Spanish proverb that says, “It’s not the same to talk of bulls as to be in the bullring.” The same applies to caring for anyone who has a chronic or terminal illness and has not lived their life as a Buddhist.
Serving Needs While Ignoring Doctrine
The way I’ve served patients for the past eight years is based more on their needs, than on many of the Buddhist principles that structure my life. I did it with someone who believed the holocaust—where thirty-nine of my relatives died in Auschwitz—was fiction. Even though I have a daughter, I listened without judgment to the sexual exploits of a former member of the Hells Angels who was released from prison so he could die in a hospice. And I did the same with countless others whose lives were examples of how not to live. The mistakes my patients made throughout their lives were powerful incentives for me to change my own, but did not alter my service to them.
Many Buddhist teachings may have limited value when the person you are caring for can only see the world and your advice through their illness. I recently experienced a pain so intense that I asked my wife to call 911. It was something unusual for me, since I have always been reluctant to seek help before trying to control my pain through meditation. But not that time. The intensity made every technique I spent years practicing as useful as a 1970s computer. Fortunately, it was nothing serious. But I learned that given a battle between the immediacy of a problem and a concept, the practicality of a problem always wins out. That was the case with one of my patients who described himself as a “confirmed atheist.”
He noticed the mala I was wearing on my wrist and asked me what it was. When I explained that it was the Buddhist version of a Catholic rosary, he asked me about Buddhism. Not in a way that was inquisitive, but rather challenging. As I struggled to explain my “practical” Buddhism using centuries-old concepts, I realized my words were sounding like the canned speeches of people who came to my door and wanted to lead me from damnation to salvation.
“I can have a monk visit you and explain it,” I said, since the San Francisco Zen Center was across the street.
“No,” he said breathlessly, an oxygen tube in his nose. “I don’t want to hear any mumbo jumbo for a professional religionist. Just tell me how what you do because of your beliefs can help me die better.”
That was the first of many interactions I had with patients who taught me to see my words and actions through their eyes—the eyes of someone who looked at the world through cancer, HIV, a chronic heart condition, early stages of dementia, ALS, or any of the hundreds of illnesses that tainted everything they felt or perceived.
If Buddhist caregivers are to be effective, they need to understand that almost everything experienced by people they are caring for is seen through the lens of their illness or the certainty of death. It’s a very different world than the one a caregiver lives in. Urging them to look at it through a Buddhist perspective, as well intentioned as it is, may be counter-productive.
Imagine being dropped into a strange country with a language you don’t understand and customs that are unfamiliar. I experienced this when I was in Prague in the Czech Republic and decided to drive to Weimer, Germany, a four-hour trip away. I didn’t speak any Czech and my German was as inadequate as it was when I studied it in high school. But I did have a GPS that guided me. Without the GPS I probably would still be wondering around Germany. In many ways, the person with a chronic or terminal illness is on a similar journey, but without a GPS.
Before their illness, how they viewed themselves was based on roles, affiliations, values, abilities, and relationships, just to mention some of the multitude of things that constitute “identity.” All of these in combination are used by people to create a picture of who they are, and by other people as they anticipate reacting to them. When an integral part of a person’s life is lost, identity changes, and so does their self-perception and place in the world.
Even though you, as a Buddhist, may believe that the stripping away of ego-enhancing activities should bring someone closer to understanding their “original nature,” it may not for someone such as the Fortune 500 executive I cared for with ALS who became dependent on a caregiver for things seemingly as inconsequential as scratching an itch. Or the novelist with dementia known for her intricate plots, who painfully wrote about becoming lost in the supermarket she had frequented for years. Losses of ego-enhancing abilities are rarely thought of in positive terms by non-Buddhists as they face a world that is constantly changing because they are. As the world of the person requiring caregiving changes, guidance for what to do should be based more on their needs than most of the Buddhist values that are the basis of your own life.
Accept Where They Live in Time
I know that the more I remain in the present, the more aware and more appreciative I am of every day I’m still alive. But is that true for everyone needing care? Is it important for everyone to remain “aware” in the present?
For Eric, it was. He stayed in the present during the last two weeks of his life. It wasn’t out of philosophical conviction, but rather because that’s where he was most comfortable. He was dying from pancreatic cancer, had been divorced twice, had a history of drug problems, and had never been able to hold a job for long. But he had an eighteen-year-old son who was devoted to him. Eric told me his son’s love was sufficient for easing his death, and up to the time when he peacefully lost consciousness, our conversations were firmly rooted in the present.
For Mary, her dying was eased when she focused on the past. For twenty years she had been instrumental in changing the lives of poor children through an afterschool reading program. As her disease painfully progressed, she focused on her past accomplishments to make the present tolerable. In her mind, she had made a difference in the world; there was no need to regret not having a future, and the present, devoid of family or friends, was no match for the joy she experienced just by remembering the past.
Although the past and present held equal relief for these two patients, death for those living in the future did not. That was the case with an author who had made significant contributions to the field of journalism and was widely published. Though he had a list of important publications that would have been the envy of most writers, he found no solace in what he had done. With only days left to live, he kept looking for a manuscript.
“I have to finish it,” he said to me one morning. “It’s due on Saturday. What day is it?”
“Tuesday,” I said.”
“Tuesday? How many days until Saturday?”
“Five days! I have six chapters to complete. I need to find it now.” He tried to get out of bed, but was too weak to sit up by himself. Another volunteer and I gently eased him back down.
“We’ll find it for you, Bill,” I said.
We kept searching the room until he fell asleep, but we couldn’t find anything that even resembled a manuscript. Until he died two days later, the most I could offer him in the way of comfort was to sit next to him and witness his anxiety about not finishing the manuscript. After he died, staff, volunteers, and a few of his friends sat around his body and each of us spoke about the impact he made on our lives. I asked a friend who had known him for many years about the manuscript.
“What manuscript?” the woman said.
“Bill said he needed to finish a manuscript by Saturday.”
“There is no manuscript,” she said. “Bill hasn’t written anything longer than a short article in ten years.” For this gifted writer, I don’t think there could ever have been enough accomplishments.
Being stuck in a specific time frame or effortlessly migrating back and forth is based on experiences, values, and needs. For many of my patients, residing firmly in the present resulted in easier deaths. In the present they could let go of the past and relinquish the future. But for others like Mary, nothing could compare with a specific era in her past, and the longer she stayed there in our conversations and her thoughts, the happier she was. Unfortunately for others like Bill, their life was future oriented. Changing how one lives close to the end of life is possible, but difficult. Sometimes the only thing you can do is be supportive of where the person has chosen to reside.
Compassion or Understanding
As someone who spends more time with ailing non-Buddhists than Buddhists, there is one principle that guides me more than any other: compassion. Thich Nhat Hanh’s explanation of it is to think of the person in front of you as if he or she was your mother who cared and fed you when you couldn’t do it yourself. With that image in mind, being compassionate with some patients became as easy as breathing. But for others, the mother envisioned by Thich Nhat Hanh took on all the characteristics of the witch in Snow White and the Seven Dwarfs. That was the case with Clarence, who was eighty, born in Alabama, and hated Blacks, Jews, Catholics, and “them damn agitators.” As someone who was involved in the civil rights movement, whose parents were Jewish, and who’s been a lifelong activist, I stood for everything he hated. He was dying and looked to me for compassion. My convictions said, “Give it.” But I couldn’t.
There will be times, despite your best efforts, that you can’t become the compassionate caregiver you want to be. I aspired to be compassionate to Clarence. I wanted to serve him, but thought I couldn’t. I realized that when compassion couldn’t be tapped into, understanding might be. How different would I be if I had been born in Selma to segregationist parents whose great great grandparents owned slaves, and whose fundamentalist religion espoused the superiority of whites, Protestants, and the Confederate cause? It was the circumstances of our lives that had made us different. When you think you can’t be compassionate, try understanding the circumstances of a person’s life. It definitely mutes those parts of it that you find unacceptable.
What’s in It for You?
Tibetans have a saying, that to get over those things you fear most—the sharp points of your life—bring them closer, rather then pushing them away. It’s an idea that many people in Western societies view as counterintuitive. For example, some try to hide from the sharp points of aging by glossing over them, with the same degree of success that a new coat of paint has on stopping an old car’s engine from sputtering. Some who have lost physical or cognitive abilities grasp at what is gone, doing little more than increasing their suffering. And for death—probably the sharpest point of all—we hide from it as if it were a tyrannical schoolteacher coming to discipline us.
The poet, Rainer Maria Rilke, thought bringing the sharp points in our life closer was an opportunity for healing. He said that our greatest fears are like dragons guarding our heart. There are few dragons as intimidating or as capable of hiding our wisdom from ourselves as long-term caregiving. Pushing away its sharp points is like covering them with a gossamer cloak; something so porous, that they emerge at unexpected moments when a smell, word, or sight allows them to resurface.
Think about the transformative events in your life. I would guess that most, if not all, involved getting past the dragons. Personal growth doesn’t seem to occur when life is pleasant. Few people would say something like “ I turned my life around sitting on the beach in Kauai being served piña coladas by attentive wait staff.” Just as intense heat and pounding are necessary for creating the highest quality swords, so are sharp points for shaping our lives. Caregiving is one of the sharpest.
The space occupied by the caregiver and the person served is special. Some would say spiritual. Depending on someone for your continued existence creates a connectiveness that is unmatched in almost any other setting. The person is saying “I can no longer continue living without your help.” The caregiver’s response should be “I’m honored to be given an opportunity to make the last phase of your life peaceful.” And while some of the experiences are enlightening, others will be unpleasant. Coming to caregiving with compassion based on a person’s needs, rather than a doctrinaire position, will allow the dragons to surface, each providing a lesson on life and death.
This should be required reading. A dear friend of mine with terminal cancer last year went through her process in a way I know many people didn’t quite understand how to deal with. And while I knew her, and had a way to connect with her, and with the way she wanted to deal with her ever-approaching end-of-the-race, she came to me about her beliefs and traditions, and I respected those. She died in November, was buried on 22 December, and I carried her wishes out to the letter. I am honoured that she entrusted the job to me, and though I miss her terribly, I am grateful she trusted me to do what SHE wanted me to do, not what I felt was the thing to do.
Amen! What you gave to your friend is probably the most precious gift one person can give to another–your support for her end of life decisions. I’m amazed by the number of people who firmly believe that their view of end of life issues is not only correct, but should be adapted by everyone. I can’t think of anything more personal than dying, and therefore, nothing as variable. You did Great!
I finished reading your article last night and found it so good and helpful that I decided to forward a link to it to all the members of a Buddhist Caregiver sangha that I belong to. I wanted to write you because while I personally am not Buddhist your insights struck a chord with me and I wanted to thank you for such a superb reflection. I believe your conclusions and approach to caregiving apply in every way to those who aren’t Buddhist but who find themselves as a caregiver for those who are.
Metta and warm regards,
Thanks for your kind words. I’ve found that certain ideas and “maxims” on how to treat others hover above all religious and spiritual traditions, and have probably done so since man could think or fashioned a stick to clunk another person over the head. Those of us who are fortunate enough to have them filter through us in the work we do, become grateful–and also humble.
Thanks so much for sharing you thoughts and feelings. I am a born again Christian and have done caregiving for many years. I have been told that I am so “good at handling” the “difficult” clients. People often shake their heads and give me a frown when I tell them that I love the person. They can’t seem to understand how this is possible. I try to explain to them that when I say I love them that it does not mean that I agree with this persons prejudices. They fail to see that hating this person for who they are is no different than this person hating others for who they are. I try my best (rarely easy) to feel for all my client what I believe Christ would feel. We all want and need to be loved. I too feel it is an honor to be able to help someone during the last phase of their earthly life. Thanks again for a wonderful article…Laura
What a wonderful article from so many different perspectives. I would add that for people who are providing caregiving services in the home, whether it is as a family caregiver, a volunteer or a paid professional, the challenges of being on-site 24/hours/day every day are daunting. Caregiving is statistically one of the most challenging jobs as far as burn-out, depression, health issues to the caregiver and financial challenges. Every caregiver needs support and some kind of relief. There are many programs out there, funded both privately and by the government. I have found 2 great sites caregivervillage.com and caregiver.org and SCRC (Southern Caregiver Resource Center). I am not affiliated with any of these organizations but as an elder-care service provider I try to pass along resources whenever possible. The most important element to having continued quality support to anyone is that the caregiver him/herself practices self-care – without that, the caregiver will not be able to be at their best, which means the level of care goes down. Great article! Judy B. http://www.elder-care-services.com
Thanks for the kind words. I agree with you, 24/7 caregiving is incredibly difficult and I doubt those who haven’t done it can fully understand. Thanks for the two references, I’ll definitely visit both sites.
Very powerful and poignant article. Would love to chat with you in greater detail about it. Haircut 11/19 @ 1030. Are you available for lunch or something?
Thanks for your kind words. I’m always available to talk with you. Lunch sounds great. I’ll email you directly.