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47 pages 1 hour read

An Unquiet Mind

Nonfiction | Autobiography / Memoir | Adult | Published in 1995

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Part 4, Chapters 10-13; EpilogueChapter Summaries & Analyses

Part 4: “An Unquiet Mind”

Part 4, Chapter 10 Summary: “Speaking of Madness”

This chapter tackles the issue of language when writing about mental illness. Jamison writes that she had once received a very angry letter criticizing her for using the word madness in the title of a lecture she was slated to give. Though she was resentful of the letter, she acknowledges that it did push her to think about the kind of language we use when discussing these issues. “On the one hand,” she writes, “the pain of hearing these words, in the wrong context or the wrong tone, is sharp; the memory of insensitivity and prejudice lasts for a long time,” but on the other hand, she feels that rejecting specific terms “gives an illusion of easy answers to impossibly difficult situations and ignores the powerful role of wit and irony as positive agents of self-notion and social change” (180-81).

To illustrate, Jamison discusses the terminology for her own illness. Although she has used the term manic-depressive illness throughout the text, the official contemporary diagnosis, according to the DSM (at the time of her writing), is bipolar disorder. However, she feels that the term bipolar suggests a distinction between that disorder and simple depression “that is not always clear, nor supported by science,” and that it further “perpetuates the notion that depression exists rather tidily segregated on its own pole,” which “flies in the face of everything that we know about the cauldronous, fluctuating nature of manic-depressive illness” (182). Further, she suggests that the destigmatization of mental illness occurs more due to aggressive public awareness measures than mere changes in terminology, including efforts by major mental health advocacy groups (183). 

Part 4, Chapter 11 Summary: “The Troubled Helix”

Jamison begins this section focused on Jim Watson, the Nobel Prize winner and coauthor of the paper explaining the structure of DNA. Watson exhibits the same kind of manic energy the author often experiences, and recently (at the time of her writing) had turned toward investigating manic-depressive illness. The illness has a rather well-defined genetic component, and in her meeting with Watson, the two examined numerous family trees demonstrating the connection.

At one point during the meeting, Jamison thinks about a conversation she had had with Mogens Schou, who is primarily responsible for the introduction of lithium as a treatment for manic-depressive illness. The two had once skipped a day of American Psychiatric Association conferences at their annual meeting in order to enjoy New Orleans, and the conversation had turned to Jamison’s interest in mood disorders. She was initially hesitant, but he explained that his interest stems from the prevalence of the illness in his own family; this caused her to open up about her own illness, which led to the creation of a similar family tree in which she noted that her mother’s side seemed to be free of manic-depressive illness while her father’s side was filled with it. She considers that she owes her life to the fact that Schou’s family tree looked similar, which pushed him to find a treatment (190).

Jamison then describes her experience with a physician recommended by a colleague many years prior. In discussing her illness, the physician had condescendingly informed her that, due to her illness and its genetic component, she should not have children. This made her feel “sick, unbelievably and utterly sick, and deeply humiliated” (191); however, she retained her composure, eager to avoid giving him further fuel. “Brutality takes many forms,” she writes, “and what he had done was not only brutal but unprofessional and uninformed. It did the kind of lasting damage that only something that cuts so quick and deep to the heart can do” (191). After all, she writes, even in her “blackest depressions,” she had “never regretted having been born” (191). Jamison, however, never did have children, as Richard already had three children from a previous marriage by the time they married; she writes that this “is the single most intolerable regret of [her] life” (192).

From there, she considers what finding the genes for manic-depressive illness might mean. On the one hand, earlier detection might be beneficial to those who do suffer from the illness. On the other, she wonders if parents will simply choose to abort children who test positive for the gene; further, she fears that eliminating manic-depressive illness might serve only to make society more homogeneous. She argues that “manic-depressive illness can confer advantages on both the individual and society,” as it “appears to convey its advantages not only through its relationship to the artistic temperament and imagination, but through its influence on many eminent scientists, as well as business, religious, military, and political leaders” (194). 

Part 4, Chapter 12 Summary: “Clinical Privileges”

Although Jamison has often, and until this point, experienced kindness and compassion when divulging her illness, she writes here about a former colleague, whom she calls “Mouseheart,” who did not show her such kindness. While living in Los Angeles, the two would frequently get coffee or lunch together, and as she grew closer to him, she felt it was important to tell him, as “Not talking about [it], if only to discuss it once, generally consigns a friendship to a certain inevitable level of superficiality” (200). Upon telling him, she discovered that he was angry with her for having attempted suicide, and that “His pain at hearing that [she] had manic-depressive illness was […] far worse than [hers] at actually having it” (200). He then questioned her ability to handle academic life, which, as she pointed out, she had already been handling for some time, by some measures considerably better than he was. Although he attempted an apology the next day, the damage had already been done.

Following this anecdote, Jamison discusses her further concerns with divulging her illness, in particular around the professional concerns thereof. Initially, she was concerned that she would not be granted a medical license if it came to light that she was manic-depressive; she built in safeguards for herself to ensure she’d be able to argue a strong case against this, but then feared that her “residents and interns may, in deference to what they perceive to be [her] feelings, not say what they really think or not ask the questions that they otherwise should” (203). Further, she is concerned that writing about her illness would make other researchers believe she is biased in her academic writing about the illness. Lastly, she wonders if, as “Mouseheart so artfully managed to” ask, if she believes “someone with mental illness should be allowed to treat patients” (204).

All of these concerns hung over her head when she applied for clinical privileges at Johns Hopkins, as part of the application asks if the applicant is “suffering from, or receiving treatment for any disability or illness” (205). Rather than answer outright on the application, she wrote that she would discuss that personally with the chairman; however, fortunately, the chairman already knew about her illness, then asserted that their faculty would be much smaller and much more boring if it had no manic-depressives (209). 

Part 4, Chapter 13 Summary: “A Life in Moods”

In this final chapter, Jamison ruminates on what it means to have lived her life with manic-depressive illness. In particular, she considers the bittersweet nature of such a life, her “longings for an earlier age” when she was “gliding through starfields and dancing along the rings of Saturn,” balanced with her current “comfortable and settled present existence” (211). She reckons that her memories are akin to a soldier’s memories of war in their vividness and discomfort: she does not “feel compelled to re-create the intensities,” yet still feels that “the seductiveness of these unbridled and intense moods is powerful; and the ancient dialogue between reason and the senses is almost always more interestingly and passionately resolved in favor of the senses” (212). Though she is “optimistic about remaining well,” she also evaluates the psychiatric wards at other hospitals and ranks them just in case she ever does slip again (212-13).

“We all build internal sea walls to keep at bay the sadnesses of life,” she writes, “and the often overwhelming forces within our minds […] through love, work, family, faith, friends, denial, alcohol, drugs, or medication”; the trick is to build them at just the right height so as to simultaneously keep people out and let them in when necessary (214-15). In writing this book, she has begun to understand that it’s less about moods or illness and more about “love as sustainer, as renewer, and as protector” (215). 

Epilogue Summary

Jamison concludes by posing the question of “whether, given the choice, [she] would choose to have manic-depressive illness” (217). She acknowledges that she can afford to pose this question at least in part because lithium is available and does work for her. She believes that “would not go through an extended [depression] again” as “There is nothing good to be said for it” (217). She dispels the idea that others who “have gone through a divorce, lost a job, or broken up with someone” know what depression is like because “these experiences carry with them feelings” whereas depression “is flat, hollow, and unendurable” (218). However, she also believes she has “felt more things, more deeply; had more experiences, more intensely; loved more, and been more loved” as a result of her manic-depressive illness (218). Because of the depth of her experiences while manic, she feels, she “cannot imagine becoming jaded to life, because [she knows] of those limit corners, with their limitless views” (219). 

Part 4-Epilogue Analysis

Although the final section of the book is still firmly written from Jamison’s perspective, Part 4 differs from the previous sections in that the emphasis in many respects is outward- rather than inward-facing. Jamison here tackles themes to which she has alluded previously, but which may not have been developed as fully, including terminology, societal expectations, genetic components, and unsupportive relatives, among others. In some ways, she uses this section to more fully elaborate upon these themes; more, though, she uses the section to move the conversation beyond herself and toward both a larger and more forward-thinking perspective. 

For example, throughout the text, Jamison has largely brought in examples of people who have been supportive of her through her illness. (One notable exception is that of her sister, but even there, it’s implied that her sister meant well, and further that she was really echoing Jamison’s own beliefs.) In “Clinical Privileges,” however, Jamison uses the example of her colleague “Mouseheart” to show why it is difficult for her to let even people she trusts in on her illness; here was a person she felt she could trust, and he betrayed that trust by blaming her for her own illness and its consequences. As an isolated example, it helps us better understand her own mindset, but she also connects this to larger possible consequences by using that experience to connect to the later experience of applying for clinical privileges at Johns Hopkins.

In both instances, we see how illness complicates matters in ways difficult for someone without such obstacles to understand. In this way, Jamison’s larger implication is that when an individual suffers from an illness such as manic-depression, it touches areas of their life that most would take for granted. (Fortunately, the latter example also serves as a counterpoint to “Mouseheart,” as the chairman not only accepts her, but even normalizes it to an extent.)

Similarly, in “The Troubled Helix,” Jamison anchors a discussion of the genetics of the illness in her own experiences, but takes the discussion beyond those experiences, as well. She began the book by discussing her father’s moods, and the genetic component was a part of the discussion throughout the text; further, we do understand that she is drawn to psychiatry and mood disorders in part because of her own struggles. “The Troubled Helix” takes this further, though, in several important ways. First, we receive a more detached, clinical understanding of the effect genetics has on the illness, as we see that her father’s side of the family is filled with such examples. Second, in Morgens Schou and Jim Watson, we see other scientists who are driven not necessarily by a simple quest for truth, but just as much by a need to understand themselves and their own experiences, which deconstructs the idea that the cold logic of science is somehow separate from human experience (and vice versa). Lastly, both here and in the other chapters of the section, Jamison uses all of this in order to question what the future might hold for our conceptions and treatment of mental illness. 

Finally, she turns all of this back inward in the Epilogue, raising the question of regret (insofar as one can, given her lack of choice). In “The Troubled Helix,” with an eye toward the future, she considers the possibility of eliminating manic-depressive illness and what that might mean for society; in the Epilogue, she makes the question personal and considers what that might have meant for her. Her conclusions are, unsurprisingly, similar: she considers her life to be fuller and richer as a result of her illness, even if it is also more complicated. However, the larger importance is not her own conclusions, but the connection she makes between the societal question and the personal question, illustrating the fact that these two questions are not different and cannot be treated as such: i.e., while some may view eliminating manic-depressive illness as a positive “cure” for a problematic disease, we cannot forget that doing so would also mean eliminating the very personal, individual experiences of people like Jamison. As a result, she ends by implicitly questioning not only if we would benefit from doing so, but if we even have the right to do so in the first place.

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