32 pages 1-hour read

On Death and Dying

Nonfiction | Book | Adult | Published in 1969

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Chapters 3-7Chapter Summaries & Analyses

Chapter 3 Summary: “First Stage: Denial and Isolation”

Most patients react to the news of their impending death with denial: “No, not me, it cannot be true” (51). Denial is the reaction of most patients for at least some time, and usually toward the beginning of their illness. This initial denial “functions as a buffer after unexpected shocking news, allows the patient to collect himself and, with time, mobilize other, less radical defenses” (52). In the vast majority of cases, it is best to tell the patient the exact nature of their situation as soon as possible. Avoiding the topic of mortality or dancing around the issue doesn’t help. Rather, it mitigates awkwardness for the health care provider. A patient’s denial is soon replaced by at least some level of acceptance.


The author relates the case of a young married woman, mother to two small children, who was diagnosed with terminal liver disease. For almost the entire length of her illness she was in deep denial, convinced in the success of a local faith healer and later convinced by her own delusions that she was going to get better and live a normal life. Toward the end of her illness, she gradually demonstrated awareness of what was happening as she began to waste away. Due to her erratic behavior, she was an unpleasant patient for the hospital staff. Her isolation contributed to her behavior. As judged by the author, if the hospital staff had simply listened and assured the patient of their continued presence, “the patient [would have] develop[ed] a feeling of confidence that here is a person who cares, who is available, who sticks around” (58). Nurturing will break down the walls precluding genuine dialogue and acceptance. The example of this young woman demonstrated “the need to examine more closely our own reactions when working with patients as they will always be reflected in the patient’s behavior and can contribute a great deal to his well-being or detriment” (62).

Chapter 4 Summary: “Second Stage: Anger”

Once denial has been dealt with, and at least some partial acceptance has taken root, the “next question becomes: ‘Why me?’” (63). The anger that follows this questioning “is displaced in all directions and projected onto the environment at times almost at random” (64). Too often those upon whom the patient’s anger is vented don’t stop to ask why it is occurring, or what they would do in the same situation; rather, they feel resentful and angry themselves. A patient “who is respected and understood, who is given attention and a little time, will soon lower his voice and reduce his angry demands. He will know that he is a valuable human being, cared for” and will almost without exception become more amenable (65).


The author relates a case where a nurse did everything she could to avoid contact with her patient. The nurse’s lack of compassion stemmed from her own fear of suffering and death. Her behavior made the patient’s outbursts and disagreeableness unbearable. In another case, a patient who had been the controlling type all his life only became mollified when allowed to have some semblance of control, even in regard to the most trivial things: “He was able to eat again, but only after all staff and relatives stopped telling him what to do” (68).


The most complex case is illustrated by an interview with “an angry, demanding patient” known as Sister I., who took out her anger on the hospital staff (69). Those who had charge of her took it personally: “Rather than understanding the origin of her anger and resentment, people in the environment reacted to it personally and began to reject her even more in reality” (90). Once her situation and motivations were considered, those around her acted with far more empathy, leading to a complete change of the patient’s attitude.

Chapter 5 Summary: “Third Stage: Bargaining”

The stage of bargaining is often very brief, if seen at all. The patient believes they can negotiate; after all, there have been other times in life when deals have been struck and good behavior rewarded. According to Kübler-Ross: “The bargaining is really an attempt to postpone; it has to include a prize offered ‘for good behavior,’ it also sets a self-imposed ‘deadline’ […] and it includes an implicit promise that the patient will not ask for more if this one postponement is granted” (96). Those caring for patients should understand that “promises may be associated with quiet guilt, and it would therefore be helpful if such remarks by patients were not just brushed aside by the staff” (96).

Chapter 6 Summary: “Fourth Stage: Depression”

Once denial is no longer a possibility and numbness has worn off, “anger and rage [are] replaced with a sense of great loss” (97). In addition to the reality of a terminal illness are financial burdens and perhaps unemployment. Two different types of depression arrive, “reactive” and “preparatory” (98). Reactive depression is a response to the various things that are no longer in one’s control. This is easier to deal with: “An understanding person will have no difficulty in eliciting the cause of the depression and in alleviating some of the unrealistic guilt or shame which often accompanies the depression” (98).


Preparatory depression sets in as the patient prepares to face the reality of death. Here, reassurances are not helpful; neither is a false sense of comfort. What is really necessary is the ability and space to reckon with the fact of death. If the patient is allowed to express their sorrow, “he will find a final acceptance much easier, and he will be grateful to those who can sit with him during this stage of depression without constantly telling him not to be sad” (99).


Kübler-Ross gives the case of Mr. H., whose depression was exacerbated by “the lack of awareness and understanding of this patient’s needs on part of those in his environment, especially his immediate family. […] His depression paralleled his increasing weakness and inability to function as a man and provider” (100). In his interview with the seminar, he showed that he was in fact very open and honest even though the hospital staff had judged him to be uncommunicative. His hopelessness was due to his inability to grieve, in part because he had never properly grieved the deaths of his own parents and child. He wasn’t unaware of his own illness or unable to come to terms with it. Rather, “he was reviewing the meaning of his life and searching for ways to share this with the most significant person—his wife” (120).

Chapter 7 Summary: “Fifth Stage: Acceptance”

When the terminal patient has had sufficient time for reflection, acceptance can take hold: “He will have mourned the impending loss of so many meaningful people and places and he will contemplate his coming end with a certain degree of quiet expectation” (123-24). While one should not confuse acceptance with happiness or contentment, acceptance brings with it peace or calm, a desire to move into the final stage of illness and the passage from life to death. In these final moments, the patient often needs the presence of those they love: “We may just let him know that it is all right to say nothing when the important things are taken care of and it is only a question of time until he can close his eyes forever” (124).


In one example given by the author, a woman—Mrs. W.—suffered a psychotic break when her husband refused to accept her impending death: “She was angry at him for not facing it and for so desperately clinging on to something that she was willing and ready to give up” (127). She could not die in peace until her husband had come around to the reality of the situation.

Chapters 3-7 Analysis

Kübler-Ross’s outline of the five stages of grief is patient-centric. It prioritizes and focuses on patients’ needs. Her approach was pioneering. According to Ira Byock, professor of medicine at the Geisel School of Medicine at Dartmouth, doctors during Kübler-Ross’s time were celebrated for their ability to prolong a patient’s life: They made decisions and didn’t enter into a conversation with the patient. In contrast, Byock explains, Kübler-Ross wanted to understand the needs of dying patients. Her approach humanized the death process and revolutionized the way medicine was practiced: “Suddenly, how people died mattered. No longer were dying patients relegated to hospital rooms at the far end of the hall” (Byock, Ira. “Dr. Elisabeth Kübler-Ross and the Five Stages of Grief.” Elizabeth Kübler-Ross Foundation, 2003).


In her first five chapters, Kübler-Ross outlines the five stages of grief by laying out fundamental theoretical principles and appealing to firsthand accounts demonstrating the principles in action. The interviews show the complexity of the grief process. As Byock points out, the case studies illustrate how some patients progress from denial to acceptance. Yet Kübler-Ross does not simplify things, he says. She shows that the process is not always smooth or linear: “We learn that some people move through denial or anger only to have these emotional states later recur as illness advances. Emotional life is complex, and the interviews in On Death and Dying reveal that sometimes seemingly incompatible states, such as denial and acceptance, can coexist” (Byock).


Denial in the patient often stems from the fear of facing pain and the prospect of leaving behind unfinished business. For parents especially, the pain of leaving behind small children to whom one has been wholly devoted can be the most painful aspect of death. Denial will often result in isolation, which will only exacerbate emotional pain. Caregivers must be observant and recognize signs signaling a patient’s needs. After denial comes anger: Patients mete out rage to those in closest proximity, be it locally or relationally. The patient projects their anger onto the world. They feel envious of the joy and health of others.


Respectful listening will often quell angry outbursts. If a nurse or caregiver feels unable to deal with the patient’s anger or resentment, then the patient can feel all the more abandoned and upset. It is essential that caregivers show empathy for those in these final stages of life and death. Empathy will often lead to the breakdown of various psychological and emotional barriers.


The mind associates good behavior and the making of promises with reward—hence the bargaining stage. Buried feelings of guilt over a life unfulfilled and ill-lived may bubble to the surface. What follows are the two kinds of depression, reactive and preparatory. Reactive depression is caused by fear of what is being lost and left behind: young children, a devoted spouse, a successful career, close family and friends. Comfort and words of encouragement are often helpful, such as assurances that family and children will be well cared for and will live happy and fulfilling lives. Here, encouragement and distraction will be successful because reactive depression stems from external concerns. In contrast, preparatory depression is interior and existential. It is the final obstacle on the path to acceptance. Encouragement will often be a hindrance. The patient must confront their sorrow over a life lost.


When one reaches acceptance, words are usually unnecessary. The patient desires quiet, sleep, and the presence of loved ones. This is the stage of waiting and passivity, where the individual passes into a quasi-infantile state of pure receptivity, unable to do or accomplish anything on their own; all they can do is wait and receive what comes. Here the family may struggle most as they see their loved one come to terms with a death which they themselves might not be ready to accept.

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