An Unquiet Mind

by

Kay Redfield Jamison

An Unquiet Mind: Chapter 11 Summary & Analysis

Summary
Analysis
Jamison describes sitting in a meeting about finding the genetic basis of manic-depressive illness with a group of researchers, psychiatrists, geneticists, and biologists—including Jim Watson, a scientist who, in 1953, co-authored an academic paper proposing that DNA had a double-helix structure. As Jamison sat watching Watson twitch and yawn, she wondered what he could be thinking about. She writes that they have been colleagues for a long time, and that she knows him to be an “intense and exceedingly blunt” person with a kinetic, untamable energy.
In this chapter, Jamison introduces her work alongside several towering greats of the scientific community in pursuit of an answer to the mysteries of manic-depressive illness. This shows that a huge group of people are banded together in hopes of understanding the disorder further and ending societal stigmas surrounding its sufferers.
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Lately, Jamison’s career has become increasingly entwined with the field of molecular biology as she and her colleagues have sought a scientific understanding of manic-depressive illness and its causes. 
Jamison wants to use this chapter to explore advances in other fields that might help sufferers of manic-depressive illness find new ways to understand their disorder. She knows that the only way real progress will be made on both scientific and societal fronts is through collaboration and good faith.
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Returning to the meeting, Jamison recalls watching her colleagues share, via projector, the genetic pedigrees of the families affected by manic-depressive illness being studied by the team of researchers present. Completely blackened circles represented sufferers of manic-depressive illness, while half-blackened circles represented depressive illness. Dark s’s or crosses signified those family members who had committed suicide. Jamison remembers feeling excited by the prospect that the men and women sitting with her in the room could be on the verge of a major scientific breakthrough that would help sufferers of manic-depressive illness the world over.
Seeing entire families’ pain and suffering laid out so starkly affects Jamison deeply—but also gives her a deep sense of hope that there are still answers to be found that may yet help sufferers of mental illness understand and combat their suffering. 
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After the presentation ended, Jamison found herself recalling a meeting with a Danish psychiatrist named Mogens Schou—the man responsible for the introduction of lithium as a treatment for manic-depressive illness—at an annual meeting of the APA in New Orleans. Taking a boat ride together on the Mississippi during a break in the conference, Schou and Jamison discussed their reasons for studying mood disorders. Schou revealed that his family was full of sufferers of depression and manic-depressive illness—all of his life’s research, he told Kay, had been driven by his personal investment in understanding the suffering within his own family.
Jamison’s meeting with Mogens Schou stands out in her mind for several reasons. He is a prominent psychiatrist responsible for advocating for the very drug that has saved Jamison’s very life—a fact which makes him seem trustworthy to her. As she listens to him and hears him speaking casually and publicly about his personal struggles with mental illness, Jamison begins to understand that the only way to change stigma is to fight it directly, with personal stories and reckonings from the heart.
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Kay recalls feeling “relieved” by Schou’s honesty and thus emboldened to share her own diagnosis, as well as her family’s history, with the man. The two of them drew out their “pedigrees” on napkins together, and the visualization allowed Kay to realize that all of the instances of manic-depressive illness in her family were located on her father’s side. Kay credits that afternoon with Schou as a turning point in which the man’s “aggressive” encouragement allowed her to feel free to use her own experiences in her work. 
Mogen Schou’s ability to discuss openly his own family history and personal story of mental illness helped embolden Jamison to do the same. She began to see that some of the most influential and intelligent people suffer the same trials she has—and that the only way to end stigma in society is to talk openly and without fear about one’s experiences.
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Quotes
Jamison goes on to describe the complex feelings that understanding manic-depressive illness as a genetic disorder has made her feel over the years. She discusses visiting a physician who asked whether she was planning on having children—and then told her that if she did, knowing there was a good chance she might pass on her illness to her child, she was being irresponsible. Jamison felt “sick” and “humiliated” at having her personhood and her condition regarded so cruelly. Jamison had never before questioned her ability to be a good mother. The doctor’s “cold-blooded[ness]” shocked Jamison. Jamison writes that one of her life’s regrets is having no children of her own—Richard has three from a previous marriage, and though she regrets not having children of her own, she enjoys being an aunt to her niece and nephews.
Jamison provides a personal anecdote from her own life to demonstrate just how deeply-ingrained and harmful society’s stigmas against the mentally ill can be. A medical professional who took an oath to “do no harm” and be an advocate for all his patients completely destroyed Jamison’s trust in him and offended her on a deep personal level. Jamison seems to suggest that the visit with the doctor contributed, at least somewhat, to her painful decision not to have children. She wants to show her readers just how affecting stigma can be.
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Jamison admits that she sometimes has concerns about what locating the genes that are responsible for the heredity of manic-depressive illness would mean. Better and earlier diagnoses, she says, would no doubt benefit patients—but there are dangers in prenatal diagnostic testing, and she worries that parents who learn their child carries the genes would lead to those parents choosing abortion and thus making the world “a blander, more homogenized place.” These ethical issues, she states, are difficult to solve—while manic-depressive illness derails and devastates many lives, there are also advantages to the disorder related to personality, thinking style, energy, expression, and artistic temperament.
Jamison acknowledges the prickly ethics of genetic and biological testing for mental illness—she suggests that some who fear the disorder due to societal stigmas might seek to eliminate it from the world without understanding the “advantages” that can also be a large part of the condition. Jamison wants to help people understand that a world without people of different backgrounds—not just socially and culturally but mentally as well—would be a poorer one.
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Jamison recalls attending a lecture at a psychiatry conference which she’d all but tuned out of until the speaker mentioned new updates on the research into structural brain abnormalities in sufferers of manic-depressive illness. Newly intrigued, Jamison listened as the speaker discussed studies revealing many small areas of “focus signal hyperintensities” which suggested abnormal brain tissue, the kind seen in other conditions such as dementia and multiple sclerosis. Jamison remembers feeling both excited and disturbed by the breakthrough, full of questions about what it could mean for her and her fellow manic-depressives. 
Jamison knows how much those living with manic-depressive illness can often suffer, and she hopes that new research into genetics and biology will help alleviate some of that suffering—even if it means learning something new and potentially frightening or upsetting about the mysterious inner workings of the human brain. Jamison is hopeful that any new research on these topics will help dismantle stigmas, not exacerbate them.
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Back at her new job at Johns Hopkins, Jamison began reading articles about the new brain scans which showed structural abnormalities in sufferers of bipolar affective disorders—only to find that there were “far more questions than answers” in the literature available. Many things could explain the sites of abnormal tissue, and as she digested this information, Jamison recalls being full of hope that the scientists at the forefront of the research were developing new insights into “the concept of losing one’s mind.”
Jamison is a person who loves learning and wants to understand more about herself, her illness, and how she can help alleviate the suffering of others with the same condition. She hopes that the breakthroughs her colleagues are making—whatever they might signify about the brain—will help make strides in the ways psychiatrists and psychologists can treat and alleviate the burdens of the mind.
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