Category Archives: Articles

Time-Worn Stories

In my family, people like to tell an anecdote about a favorite uncle, Bill, who had the reputation of being kind and open to everyone he met. Such was his good nature that he would greet strangers with warmth, so much so that we used to fear others taking advantage of him.

One day, it is told, Bill was coming down the front stairs inside his house. At the same time, another man, rather tipsy from imbibing too much, was walking up. Bill, according to the story, hailed the intruder with a friendly greeting, and then continued his way down and out the door.

This tale, not without fictitious added details perhaps, gets repeated often when our extended family gathers for anniversaries or other events. The younger members who have heard the story more than once are probably thoroughly bored with it by now. It’s the kind of tale that I myself in my younger days used to turn off as not worth repetition. I was looking instead for things that I had not heard before.

Now that I have reached a certain age, however, I have come to see that the telling of such stories can easily be underrated. Perhaps they amount to a rite that has great importance for the elders of the family and even for the younger members as well.

Writer James Hillman tells of interrupting his uncle in the middle of a time-worn story. “You’ve already told me that,” the nephew said. His uncle’s riposte, delivered at lightening speed, was “I like telling it.” Under his breath, the uncle probably said (as Hillman imagines), “And what the hell is wrong with telling it again? Don’t you know anything about the pleasure of telling the same stories?”

Of his uncle, Hillman adds, “He knew the pleasure of the groove.” He goes on to suggest that it is shortsighted to judge repetition as an addiction. “Why not, instead, conceive of the need for novelty as an addiction?” he asks.

In exploring the time-honored story, this Jungian analyst suggests that the story genre causes boredom only if you listen to it for facts. If, for example, grandmother tells about a fire that almost destroyed her house and details who did what to escape, the mere facts might leave listeners cold.

However, Hillman says, “The story is also a lesson about concealed dangers, about protecting ‘home,’ about family collaboration, and about the character of each of the ‘characters’ whose styles emerge through the emergency.”

Stories like the grandmother’s aim to establish a permanency that, amid the ceaseless flow of life’s events, reassure us that some things stay the same. “It is as if the soul begs for the same stories so that it knows that something will last.”

You may be tempted to dismiss this kind of analysis as the feverish speculations of an imagination run amok. But it does help me realize how superficial I can be in dismissing family rites and rituals cherished by friends. They do indeed often have the power to feed the soul and to enhance our lives.

Hillman carries it even further. “That forgetful old uncle, that tiresome grandmother offer a foretaste of the eternal. They function as ancestors, reminding us that recapitulation is the way the world really works.”

The writer concludes the matter thus: “Nothing is more tedious than practicing your scales or mumbling your beads. Yet the accomplishments of art, the efficacy of prayer, the beauty of ritual, and the force of character depend on petty repetitions any instant of which, taken for itself alone, seems utterly useless.”

If soul is what counts most, then family stories would seem to have great value indeed. Those who have cultivated “the pleasure of the groove” may have more wisdom than we think. Whether highly educated or not, they develop a sense of self-worth as tellers of the tale. They are fulfilling a role held important always and everywhere, I suspect, because it’s a powerful instrument for continuity.

If Hillman is right in suggesting that repetition does indeed point toward the eternal, then its spiritual content is even richer. “Is that all there is?” remains a potent question demanding an answer. Perhaps we can find in the traditions of family story-telling signs that point onward and upward. The actual stories may sound hokey sometimes but they can come freighted with values that we ignore only at our peril.

We could do worse than to ponder what Thomas Lynch writes in his 1998 book of poems, Still Life in Milford: “How we repeat ourselves, like stars in the dark night, / and after Darwin, Freud and popes and worlds at war, / we are still our father’s sons and daughters / still our mother’s darling girls and boys, / aging first, then aged then ageless.”

Richard Griffin

No-Trade Policy

At a recent hometown baseball game, played for charity, I happened to sit next to a man whose wife and two daughters were with him. One of his daughters who was moving around the stands animatedly, looked about twenty years old; the other, whom I will call Eleanor, seemed several years younger.

On being introduced to her, I quickly realized that Eleanor could not talk. She tried to, but could only make inarticulate noises. Sometimes she moaned and seemed to be in distress but her parents did not get upset. Throughout the evening, she sat next to her father and would occasionally rest her head on his shoulder.

In conversation with the father, I discovered from him that Eleanor has a rare disease that prevents some children from developing normally. She was born with this affliction and thus has had to live with it her whole life.

So have her parents. Clearly, they have given this daughter devoted attention. Her needs have been a priority for them and they have made her feel loved. I became convinced of this love when the father told me: “I would not trade her for the world.”

This statement struck me as evidence of a deep spirituality that has taken root in this man’s life. His words have stayed with me since that evening, three weeks ago, and have continued to impress me with their beauty. Though I do not know the man’s name and have failed in my efforts to trace him for an interview, I can imagine how Eleanor’s life has shaped his own and that of his wife.

At the beginning it must have come as a shock. For them to realize that this child was born with severe disabilities would have upset their expectations and made them wonder how this could have happened. If they were believers, their faith in God may have been shaken making them doubt, for a time, that God still cared for them. “Why us?” they probably asked. They may even have fantasized about exchanging their child for one that was whole.

They must have felt anxious for their child as they consulted medical specialists, experts in the disease, to discover what could be done. Surely, they must have thought, some new medical technique or wonder drugs might at least alleviate the effects of the ailment.

At a certain point, they would have accepted the inescapable fact that Eleanor would always be severely limited in what she could do. No matter what, this child would never be able to talk or to be independent. She would need her parents to take care of her as long as she, and they, lived.

One can imagine how this realization would have required a recasting of imagination and emotion. These parents would have been forced to think differently about their child’s future and their own. They would find themselves in spiritual crisis, needing to adjust their hopes and dreams to the reality thrust upon them.

From all appearances, they have met this crisis bravely and learned how to become different parents from what they must have expected to be. With courage, patience, and hope, they have apparently learned to face a transformed future as they have come to grips with a situation so different from what they ever thought possible.

Above all, they learned love in a new way. If a strong spirituality has taken root in these parents the way I believe, it is most of all because of their love. And though this love is directed toward their daughter Eleanor, it must have strengthened the bond between them as marriage partners and, indeed, the bonds with their whole family.

Again, the father’s statement reverberates in me: “I would not trade her for the world.” Those simple words carry a love that has been wrested out of severe reality. This line conveys a hard-won spiritual maturity that gives deep meaning to his life and that of his wife.

As a lay theologian writes in this week’s issue of Commonweal, “I am increasingly convinced that my relationship with my wife, and with our children, is the spiritual ‘place’ where I will work out my salvation.” The theologian’s language might strike Eleanor’s father as foreign but it may express something of the same spiritual reality that he, too, is living out.

Richard Griffin

Diane Meier et al

Diane Meier, M.D., buys tall stacks of paperback editions of Tolstoy’s classic story, “The Death of Ivan Ilyich.” This she does so that the students, medical residents, and others whom she supervises can read this inspired account of a man who refuses to face the truth about his approaching death. She believes that this narrative can help awaken young doctors to end-of-life issues.

Dr. Meier, founder of the palliative care program at Mount Sinai Medical Center in New York City, takes a leading role in the second program of Bill Moyers’ public television series “On Our Own Terms.” This series, broadcast in Boston this week, champions what Moyers calls “a different kind of care” for people who cannot be cured of life-threatening disease.

In his famous novella centering on the dying Ivan Ilyitch, Tolstoy showed in stark detail how fatal illness devastates a man who is emotionally cut off from family and friends and from his own inner self. His pain, both physical and spiritual, is intense and he suffers a devastating crisis of belief. Only in his last moments, through the compassion of a young man servant, does Ivan discover his soul and see the darkness of his dying yield to light.

Health care pioneers such as Dr. Meier are shown in the Moyers series as leading the way toward a set of medical priorities different from those normal in the American health care system at large. They focus first on pain and work to control and relieve the suffering of their terminally ill patients. These physicians are trying to get their colleagues to recognize that pain is both debilitating and unnecessary.

Doctors are not the only ones who fail to see the importance of dealing with pain. Patients themselves often believe it undesirable to eliminate pain altogether. So do members of their families.

That’s the way it was with Matt Wilson, only 23 years old, who is shown dying at Mt. Sinai. His family fears that, if Matt’s pain is relieved, then he will lose his desire to fight for life.

Similarly, another patient, Harold Resnick, refuses pain medication at first because he is afraid that taking medication will be equivalent to resigning himself to death. Dr. Meier begins talking with these patients and their families so that they can see how relieving pain can help them cope better with their actual situation.

Watching these people wrestle with devastating illness is admittedly not easy. I have taken no pleasure in doing so, nor in writing about the Moyers series. However, I stand convinced that end-of-life  issues have crucial importance for everyone. I return to these questions, despite the fearful emotions they stir in us, because I believe that dealing with the issues in advance can increase our chances of accomplishing vital human tasks before dying.

Joyce Kerr is another Mt. Sinai patient who is dying of cancer. She decides to leave the hospital so that she can die at home. There she will have support from hospice services and from family members. Her daughter, Nancy Akbari, reasons this way: “How many nights did she sit with me, it’s just nice to be able to try and give some of that back.”

Mrs. Kerr’s doctor, Sean Morrison, visits regularly and talks with her about her experience. He also helps family members by explaining, with much compassion, what they can expect at each stage of their mother’s dying.

To make this approach to care of the dying the usual way will require drastic changes in the American health care system. Physicians, nurses, and other medical team members must learn to practice medicine differently from the way they learned it in school. They have to recognize that attention to the patient is ultimately more important than attention to the disease. Thus talking and listening become vital approaches to patient care.

These pioneers must also deal with a health care system that has different priorities. Financial incentives often act as a barrier to appropriate care. A huge number of Americans lack health insurance to cover them in times of crisis. Regulations frequently act as barriers to people getting the kind of care they need.  

But the health care reformers shown in the “On Our Own Terms” series are motivated by their conviction that the present system does not serve dying people decently. “I’ve seen too many people die in our intensive care unit in ways that you and I would never want to die,” a doctor tells Bill Moyers.

Palliative care – the relief and control of pain along with attention to the physical, emotional, psychological, and spiritual needs of dying patients – can make a vital difference in the way we die. Bill Moyers and his collaborators deserve credit for raising the issues unflinchingly and presenting, in real-life situations, professionals, patients and their families, who have the courage and wisdom to show how it can be done.

Richard Griffin

Amos Bailey

Amos Bailey M.D. took the lead in founding “Balm of Gilead,” the only hospice or comfort care organization in the state of Alabama. Along with Edwina Taylor, a nurse, and other associates, Dr. Bailey primarily serves the working poor of Birmingham and the underinsured. This health care team tries to help terminally ill people to die peacefully, with opportunities to attend to personal and spiritual issues.

These compassionate and creative medical professionals appear in the fourth section of Bill Moyers’ new series “On Our Own Terms.” The first program will be shown starting this month on public television stations across the country. Convinced of the series’ importance, the stations have mounted a major publicity drive and have organized community groups to discuss vital questions raised by the programs.

Dr. Bailey wants to change the culture of dying. His effort is to control the pain of his patients so that they can make good end-of-life choices and also attend to important personal issues. He aims at stabilizing the condition of patients so that, if at all possible, they can go home to die.

As Bill Moyers explains, that’s where most Americans wish to spend their last days. Statistics show, however, that four out or five of us die in hospitals or nursing homes. To change this reality requires reformers to go against many different obstacles, as Dr. Bailey has discovered.

At Balm of Gilead, top priority goes to relief of suffering. That includes four different kinds of suffering: physical, emotional, spiritual, and social. If physical suffering is not controlled, Dr. Bailey emphasizes, then it is impossible for patients to concentrate on anything else. But then, the other kinds of suffering pose challenges, too. As Bill Moyers says, “There are no charts for soul pain.”

Dr. Bailey and his associates like to consider control of pain as a person’s fifth vital sign, the others being blood pressure, body temperature, pulse, and respiration.

The team also is committed to avoiding invasive medical treatment such as oxygen masks that cover the face. And, for these patients, they do not recommend surgery or other drastic means for prolonging life.

These health care providers, instead, spend much of their time talking and listening. As Edwina Taylor says of her patients, “It’s such a powerful thing for them to know that they have someone standing with them, that it’s okay to talk about dying.”

John Reagan, age 85, one of Dr. Bailey’s patients, could not stay at home because he could not handle his own medications. This resulted in his being sent to a nursing home where regulations at first did not allow Dr. Bailey to continue to take care of Mr. Reagan.

Another of his patients, Mrs. James, will have to leave his care if she takes too long to die because Medicare covers only six months. Still another, Portia Boyd, needs to employ a woman to prepare meals but Medicare will not pay for this vital chore. Dr. Joanne Lynn, another pioneer in end-of –life care, is heard to complain, “I can get any patient into the ICU (intensive care unit), but I can’t get a meal delivered on the weekend.”

Another chief obstacle to a shift in priorities does not directly concern insurance coverage. Rather, it is the lack of training of most doctors in pain control and end-of-life issues. Too many of them give their main attention to the illness instead of the person. As Edwina Taylor, a nurse with 29 years’ experience says, “A lot of doctors cannot admit that a patient will die.”

Things are changing, however. One half of Americans who die of cancer now do so with the assistance of a hospice program. This fact suggests that more and more people recognize, among other things, the importance of spiritual issues as one prepares for death.

The Massachusetts Compassionate Care Coalition, a group of 140 people from forty different organizations, aims to improve care of the dying. Founded two years ago, this coalition tries to help people become aware of good end-of-life care and of the decisions that need to be made then.

Carol Wogrin, MCCC’s spokeswoman, says of those involved in this end-of-life care, “People don’t work with the dying just because they need a job; for whatever reason, they feel compelled.”

To judge from the television series, these words aptly describe Dr. Bailey, Ms. Taylor and the other team members at Balm of Gilead in Birmingham.

Richard Griffin

On Our Own Terms

Bill Bartholome, is a pediatrician who has become terminally ill with cancer. Of his discovery that he is going to die, he says, “I experienced a kind of grief that I had never known.” Television cameras follow closely the saga of his decline and approaching death as Bill chooses to forgo curative treatment in favor of relief of pain.

Bill Bartholome is only one among dozens of people the viewer meets in Bill Moyers’ new public television series “A Death of One’s Own.” This four-part series is ready to air on Boston’s Channel 2, starting on Sunday evening, September 10 and running the next three nights from 9:30 to 10:30. (The programs will be repeated in early morning hours on Channel 44.)

With Bill Bartholome and offering him loving support during his ordeal is Pam, his fiancée. At this time, she follows through and marries Bill, much to his amazement. “I could not believe that she would do it,” he exclaims.

Living day by day with the knowledge that his death is approaching, transforms life for Bill. Agonizing as this realization certainly is, it makes him appreciate living as never before. Though he says “I am in contact with the skeleton that I am becoming,” he also witnesses to  the arrival of another springtime as “an incredible miracle.”

It’s not how long you live that makes life valuable, Bill comes to see.  When his death comes, some months after we first meet him, he has arrived at a certain level of peace. “Thanks for letting me care for you,” Pam told him then, knowing that he would no longer be able to argue against this sentiment of hers. At that point she was grieving for him, experiencing what writer and professional undertaker Thomas Lynch says by way of commentary, “Grieving is the tax on loving people – the intimate contract.”

These programs are not always easy to watch. As Moyers himself admits, “It’s not pretty, looking at a dying person.” My own emotions, as I went through preview tapes, ran the gamut from pity for others to fear for myself, with many stops between. Often my eyes watered as I saw what happens to many dying people, especially those who suffer added burdens of poverty and isolation.

It is hard to know whom to admire most. The patients who struggle to preserve dignity amid end-of-life crises certainly stir respect, among many other responses. But so do members of the health care staffs – physicians, nurses, aides, hospice workers, and others – who struggle to relieve pain and help patients die with some degree of peace.

Dying this way is denied to altogether too many Americans. Surveys show that most of us want to die at home. However, the stark reality is that four out of five of us actually die in hospitals or nursing homes. And, even worse, many of us die in pain that could and should be controlled and relieved. One of Bill Moyers’ prime reasons for creating this series is to change the American way of death.

Some of the doctors one meets in this series are trying to do this, while struggling against the force of the medical establishment and national priorities. The pioneering physicians shown here, along with their nurse collaborators and other professionals, display both deep sympathy with patients and their families, and, at the same time, passionate disapproval of the system under which they have to work.

A wonderfully compassionate nurse named Edwina Taylor says of her dying patients, “That’s the greatest gift you can give to a person, is to really listen.” Diane Meier, a physician who started the palliative care unit at Mount Sinai Medical Center in New York City, says of her nine years of medical training, “ I did not have a single lecture in pain management.”

Greg Gramelspacher, a doctor who works with poor people in Indianapolis, says, “I’ve seen too many people die in our intensive care unit in ways that you or I would never want to die.”

And Amos Baily, a youthful-looking, marvelously sympathetic doctor in Birmingham, Alabama, is trying to introduce palliative or comfort care, into the mainstream of medical practice there. “I saw bad things happening,” he comments, and I wanted to fix it.”

The first patient mentioned here, Bill Bartholome, said of one group of his care providers, “Dying without hospice is like having surgery without anesthesia.” As if in commentary, the founder of the Zen Hospice Center in San Francisco, Frank Ostaseski, says of hospice work, “We’ve been doing this with each other for hundreds of years – we’ve just forgotten.”

Bill Moyers thinks the time is ripe for radical change. If we are to improve the chances for a good death, citizens must act now. Moyers hopes that discussion groups all around the country will form to talk about the issues and to plan agendas for change.

This column can provide little more than an introduction a series rich in detail.  More information is available at 800 962-2973. Related material can be found on the web at http://www.pbs.org/wnet/onourownterms/community/index.html.

Richard Griffin 

Moyers Series

“I experienced a kind of grief that I had never known.” This was how Bill Bartholome of Kansas City spoke about discovering that he was going to die from cancer of the esophagus. “The pain was not in the same league as the suffering,” he went on to explain, “but, you move down the road, and it becomes okay.”

This statement comes from the first segment of Bill Moyers’ four-part, six-hour blockbuster television series called “On Our Own Terms.” This series, which carries the subtitle “Moyers on Dying,” will be shown this month on many public television stations across the country.

Boston’s Channel 2 will broadcast it, September 10 through 13, at 9:30 in the evening.  New Hampshire’s Channel 11 will show the first two parts at 9:00 PM on September 16 and the last two on September 23. Both stations have scheduled repeat showings at other times, with Boston’s airing on Channel 44.

For people concerned about end-of-life spiritual issues, as well as the whole range of medical and other subjects connected with death and dying, this series deserves careful watching. Previewing the tapes as I have done enables me to recommend it enthusiastically as a uniquely valuable and moving experience.

It is by no means always easy to watch. Viewers are shown real-life scenes of human suffering and the devastation wrought by disease. At the same time, one also comes close to the beauty of the human spirit, – the courage and devotion of people who undergo the experience of dying and of those who serve them. There were times in the series when I felt tears come to my eyes and when I felt stirred to admiration of my fellow humans.

Bill Bartholme, himself a physician, is among the first persons whose dying is traced in this fine documentary. Though he was himself a full professor in his medical school and attached to its hospital, “his experience as a patient was devastating.” No one among the medical personnel took his pain seriously and, at  a time when he needed attention, he was left to fend for himself on a cot in a hospital corridor.

Vital to his functioning in his last few months of life was the decision of his fiancée, Pam, to marry him. “I could not believe that she would do it,” said Bill. But for Pam it was an expression of a love that could not be damaged by the prospect of Bill’s death but only strengthened.

They decide that, for Bill, treatments aimed at a cure do not make sense. Instead, they instruct their medical team to focus on the relief of pain and on other measures to help him prepare for a good death.

In the meantime, Bill finds that the knowledge of death’s nearness enhances his experience of living. “If you don’t expect to see spring when fall comes and then you are around and get to see spring,” he says, “you don’t experience it as spring. You experience it as a miracle.”

Throughout the running time of six hours, one meets other people who are facing death in the near future. And one gets to know physicians, nurses, and other medical professionals who are trying to change the way in which hospitals and individual caregivers provide services to the dying.

Some of these professionals belong to so-called palliative care teams that make it their business to deal with the pain and discomfort of patients for whom a cure is no longer realistic. I found it inspiring to see such professionals going against the system to defend the rights of their patients to die without undergoing further treatments that cannot help them and may possibly increase their suffering.

Bill Moyers and his collaborators have announced ambitious goals for this series. They want to begin a national conversation about improving the way  Americans die. They hope to spark discussion all across the country about the issues that surround death and dying.

The crucial issues that the series takes on include the following: fear of dying in pain; concern about being a burden on family and loved ones; acute financial stress; fear of dying alone; loss of control and dignity.

A free information packet is available. To get it after the broadcast, you can call 800 962-2973. You can also find material on the web at http://www.pbs.org/wnet/onourownterms/community/index.html

Richard Griffin

Jin Shin Jyutsu

Most therapeutic techniques that are employed to promote relaxation hold little attraction for me. For years, I have failed to profit from controlled breathing, for example, a practice that works for many other people. Even meditation, which I have long practiced within the classic tradition of western spirituality, does little to relieve my anxiety or to soothe bodily stress.

For this reason, I felt somewhat wary in accepting a longstanding invitation from one of my readers, Phyllis Reichart of Watertown, to experience Jin Shin Jyutsu, the therapeutic technique that she practices. This 42-year-old single mother is a certified practitioner of what her brochure describes as an “ancient energy-harmonizing art that can help reduce stress and promote health and well-being.”

Jin Shin Jyutsu traces its origins to ancient times in Japan. However, it fell into obscurity for centuries until rediscovered in the early 1900s by a Japanese master who devoted his life to its development. In the 1950s, it was introduced to the United States by a woman named Mary Burmeister who took the lead in spreading it around this county.

Phyllis Reichart became involved in this therapeutic practice five years ago after having pursued a career as an educator. Her motivation has been to help people to find more peace of soul and body. Older people like me, she believes, can profit from this discipline, especially if they are experiencing symptoms of tension or illness for the first time.

Given my misgivings about such practices, I agreed to take part in this exercise somewhat warily but in the spirit of adventure. Though Jin Shin Jyutsu was entirely new and unknown to me, I trusted that it would do me no harm, and might possibly deliver on some of its promises. It helped greatly that Phyllis Reichart was so patient in answering the questions of this first-time wayfarer.

It is gratifying to report here that the one-hour session introducing me to this Japanese art proved both enjoyable and, as I hoped, relaxing. To my surprise, it also turned out to be subtly and agreeably energizing as well. For the next couple of days I felt my spirits notably higher than usual.

These positive results emerged even though I remain, if not dubious, at least agnostic about the rationale behind the art. This explanation attributes undesirable physical and mental symptoms of stress to “blocked energy flows.” It believes that these blockages can by opened by making contact with certain  pressure points on the surface of the body.

Practitioners begin this exercise by feeling your pulse to determine your current flow of energy and state of well-being. Then, by gently placing their hands on “Safety Energy Locks” located at various bodily sites, therapists can begin to clear out energy blocks and you can start to experience “renewed vitality and harmony.”

As already noted, personal lack of faith in this explanation of bodily dynamics did not prevent me from enjoying the whole experience. From the beginning, when I lay down on the table, after removing only my shoes and wristwatch, I felt the practitioner’s touch as soothing and the procedure agreeable.

The therapist does not do any massage nor manipulation of muscles. Instead she proceeds by merely placing either her fingertips or her whole hand on each the body’s 52 primary locations (26 on each side.)

Phyllis Reichart showed herself gentle and sympathetic throughout as I submitted to this unfamiliar process. At several points, she explained what she was doing in order to allay whatever anxiety I might have felt as a beginner. Restful music played nearby. From an adjoining room I could hear Phyllis’ four-year-old daughter happily playing under the supervision of a caretaker.

Before moving her hand to each new site, Phyllis would try to sense when the vital energy had been successfully harmonized with the previously opened locations. These points on the body, by the way, correspond almost identically to the sites used in acupuncture and other such disciplines.

At the session’s end, Phyllis gave me materials designed to help me carry on the therapy on my own. One is entitled “Harmonizing of Attitudes through Fingers” and indicates “how to get rid of worry fast.” Though I welcome anything that can relieve anxiety quickly, long experience makes me doubt that such a thing is possible.

Later years, I believe, are favorable times for “experimenting with truth.” This phrase of Gandhi first gave me inspiration long ago and continues to do so now.

This Gandhian framework I use in evaluating my brief experience with Jin Shin Jyutsu. It introduced me to a new and different worldview. It opened up a new approach for coping with stress, adding to already familiar methods. It revealed more of the mysterious connections between the spiritual and the physical sides of human existence. And it showed me once again the beauty and power in human touch.

Anyone wishing for more information about this therapy can tap into its web site at www.jinshinjyutsu.com. [link no longer active]

Richard Griffin