The mind's eye

Oliver W. Sacks

Book - 2010

Includes stories of people who are able to navigate the world and communicate with others despite losing what many of us consider indispensable senses and faculties: the power of speech, the capacity to recognize faces, the sense of three-dimensional space, the ability to read, and the sense of sight. This book is a testament to the complexity of vision and the brain and to the power of creativity and adaptation, and it provides a whole new perspective on the power of language and communication, as we try to imagine what it is to perceive through another person's eyes, or another person's mind.

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Subjects
Published
New York : Alfred A. Knopf 2010.
Language
English
Main Author
Oliver W. Sacks (-)
Edition
1st ed
Item Description
"A Borzoi book" -- T.p. verso.
Physical Description
xii, 263 p. : ill. ; 22 cm
Bibliography
Includes bibliographical references (p. [241]-252) and index.
ISBN
9780307272089
  • Sight reading
  • Recalled to life
  • A man of letters
  • Face-blind
  • Stereo Sue
  • Persistence of vision: a journal
  • The mind's eye.
Review by Choice Review

The Mind's Eye, like other books (e.g., Musicophilia, CH, Apr'08, 45-4287) by eminent neurologist Sacks (Columbia Univ. Medical Center), explores the linkages between brain and behavior. It evaluates visual processing, particularly its deprivation and the body's responses to this. Sacks examines the consequences of aphasia (problems recognizing language), prosopagnosia (difficulty interpreting faces), loss of stereopsis (seeing depth with both eyes), and finally, partial (one eye) or complete blindness. Rather than just looking at the results of damage or disconnection, the book focuses on what happens after--on learning, reorganization, and the compensation that people make when their sensory world is so disrupted. Despite what looks like terrible lack or loss, a person can rise above the deprivation and lead a full and, in some cases, distinguished life. Not everyone reacts the same way; for instance, some blind people are excellent at visual imaging; others can apparently "write" on a visual "screen"; still others shift their focus to other senses and enhance them. This intriguing account of plasticity is interwoven with historical asides about visual theorists along with some of the author's own experiences. It makes a fascinating mosaic reflecting how brain and behavior work and a ringing endorsement of the human spirit. Summing Up: Highly recommended. All levels/libraries. J. A. Mather University of Lethbridge

Copyright American Library Association, used with permission.
Review by New York Times Review

THOSE whose familiarity with Oliver Sacks extends only to his vivid book titles - "The Island of the Colorblind," "An Anthropologist on Mars," "The Man Who Mistook His Wife for a Hat" - may picture his writing as a gallery of grotesques, a parade of the exotically impaired. Sacks, a practicing neurologist, does specialize in case studies of highly unusual patients. But even as he entertains and diverts with his dramatic tales, Sacks has always been up to something else: he is gently educating us about the frailties and flaws - and the strengths and capacities - of "normal" people, those whose afflictions are of the most ordinary sort. You may never have confused your spouse for an item of outerwear, but have you ever failed to recognize the face of an acquaintance? Fumbled for a word that eluded your grasp? Read a sentence three times and still didn't get it? Such familiar slips, and how we handle them, are the stealth subjects of Sacks' latest book. "The Mind's Eye" is a collection of essays - some of which have already appeared in The New Yorker - but it has a remarkably graceful coherence of theme, tone and approach. Once again, Sacks explores our shared condition through a series of vivid characters: the woman who couldn't talk, the man who couldn't read, the "prosopagnosic" who couldn't identify her own face in a photograph. (For those who wonder just how Sacks locates such people, it soon becomes clear that many of his patients find him, after recognizing themselves in his writing. They enter his care through the pages of his books, and in turn become characters in his next round of stories.) The sufferers who write to Sacks receive a deeply empathetic response. Of one correspondent, a woman who has lost the capacity to read (but, remarkably, retains the ability to write), Sacks notes that he responded to her by telephone. "I normally would have written back " he tells us, but in this case calling "seemed to be the thing to do." Over time this patient, afflicted with a degenerative brain condition called posterior cortical atrophy, loses her ability to recognize objects and people, though she retains a keen sense of color and shape. When Sacks meets her in person to see how she navigates her everyday life, he dresses head to toe in red so she can keep track of him in a crowd. Given to such un-self-consciously generous gestures, Sacks would seem to be the ideal doctor: observant but accepting, thorough but tender, training his full attention on one patient at a time. For the patient's benefit and for ours, he illuminates every uncanny detail, brings out every excruciating irony. The woman for whom Sacks dresses in red, for example, is a virtuoso pianist, and the first sign of her malady is a sudden inability to read music. She is joined in these pages by a novelist who wakes up one morning unable to read, and an intensely sociable woman who is suddenly struck dumb. But Sacks is not primarily interested in documenting pathology, or even curing disease, which in most cases is impossible. There are no miraculous "awakenings" here. Rather, he is most engaged by the process of compensation, how people make up for what they have lost, wresting new possibilities from their newly imposed limits. There's the blind man who develops super-sensitive hearing, the deaf woman who catches tiny shifts in facial expression - and that pianist, who loses her ability to read music but gains new richness in her thinking about music. "She felt that her musical memory, her musical imagery, had become stronger, more tenacious, but also more flexible, so that she could hold the most complex music in her mind, then rearrange it and replay it mentally, in a way that would have been impossible before," Sacks writes. Sometimes these compensations are biological, he explains. The brain, plastic even into adulthood, reshapes itself to fit a new reality. In people who become blind as adults, Sacks notes, the part of the brain that once processed visual information does not atrophy, but is reallocated for another use. "The visual cortex, deprived of visual input, is still good neural real estate, available and clamoring for a new function." At other times, compensation takes the form of an ingenious tool. The social butterfly rendered mute by a stroke uses a lexicon, a book full of words to which she can point. (The lexicon is devised for her by a speech pathologist who is herself, Sacks notes in passing, a quadriplegic.) The novelist employs a journal-like "memory book" to teach himself how to read again. Such tools can help forge a new whole from patients' shattered identities. As the novelist puts it, "The memory book returned a piece of myself to me." Sacks is most attuned to the psychological and emotional adjustments patients make to their new status; he clearly admires how they have gone on "to develop other ways of doing things, capitalizing on their strengths, finding compensations and accommodations of every sort." In her piano playing, Sacks writes, the woman who could no longer read "not only coped with disease, but transcended it." So rewarding are the compensations of Sacks' patients, in fact, that we begin to feel as if the tragedies that befell them were not tragedies at all, but - as the self-help books say - opportunities for growth. Then we arrive at the book's penultimate essay, about Sacks' own ocular cancer. His story is told in journal entries, dated from December 2005 to December 2009, which take on a deepening urgency as we experience along with him one event after another: the strange symptoms, the grim diagnosis, the painful treatment, the halting, incomplete recovery. Sacks' jaunty confidence and sanguine attitude disappear, replaced by a panicked and sometimes piteous voice that is new to the reader and (if I may be so ungenerous) quite unwelcome. On Dec. 25, 2005, he writes: "Everyone says 'Merry Christmas!' and I reply in kind, but this is the darkest Christmas I have ever known. The New York Times today has pictures and stories of various figures who have died in 2005. Will I be among those figures in 2006?" I found myself longing for the return of the ideal doctor of earlier chapters, and then I saw. He was right there, teaching us one more lesson: that compensation is meager consolation, that loss is painful, no matter what replaces it. Even those of us who have never lost our sight or faced a cancer diagnosis know how profoundly unsettling change can be. A move to a new job or a new neighborhood may make us, for a time, full of complaint and self-pity. It is characteristic of Sacks' generosity to his patients that he allows only himself to be seen in this light. Yet Sacks does eventually rally, his playful spirit intact. He notices that the blind spot, or scotoma, in his tumor-stricken right eye resembles the shape of Australia, "complete with a little bulge in the southeast corner - I thought of this as its Tasmania." He observes that if he keeps his gaze steady for a few moments, his brain will "fill in" his blind spot with imagery borrowed from the parts of the scene he can see. The ever resilient brain, he remarks, "does not just fill in color, it fills in patterns too, and I enjoyed experimenting with my own scotoma, testing its powers and limitations." Sacks calls this activity "scotomizing." Irrepressible though he may be, Sacks will not let us forget the sober lesson of his experience. He ends the essay not with a cheering paean to human resilience, but with a bleak new turn of events. A hemorrhage has further clouded his vision, leaving him with a gaping "nowhere" in his right visual field. "Time will tell whether I am able to adapt to this new visual challenge," he writes. Perhaps Sacks will take comfort from his novel-writing patient, who with great effort taught himself to read again. "The problems never went away," the novelist reports, "but I became cleverer at solving them." Sacks is most engaged by the process of compensation, how people make up for what they have lost. Annie Murphy Paul is the author of "Origins: How the Nine Months Before Birth Shape the Rest of Our Lives."

Copyright (c) The New York Times Company [November 14, 2010]
Review by Booklist Review

Sacks, famous for combining his knowledge as a physician and his compassion for human stories of coping with neurological disorders, offers case histories of six individuals adjusting to major changes in their vision. A renowned pianist has lost the ability to read music scores and must cope with the fear of an ever-shrinking life as her vision worsens. A prolific writer develops word blindness and is unable to read even what he himself writes, forcing him to develop memory books in his mind, adaptations that he later incorporates into his fiction writing. Sacks recalls his own struggle to cope with a tumor in his eye that left him unable to perceive depth. He includes diary entries and drawings of his harrowing experience. Sacks, author of the acclaimed Musicophilia (2007), among other titles, combines neurobiology, psychology, and psychiatry in this riveting exploration of how we use our vision to perceive and understand the world and our place in it and how our brains teach us to see those things we need to lead a complete, fulfilled life.--Bush, Vanessa Copyright 2010 Booklist

From Booklist, Copyright (c) American Library Association. Used with permission.
Review by Publisher's Weekly Review

Sacks, a neurologist and practicing physician at Columbia University Medical Center, and author of ten popular books on the quirks of the human mind (The Man Who Mistook His Wife for a Hat) focuses here on creative people who have learned to compensate for potentially devastating disabilities. From the concert pianist who progressively lost the ability to recognize objects (including musical scores) yet managed to keep performing from memory, to the writer whose stroke disturbed his ability to read but not his ability to write (he used his experience to write a novel about a detective suffering from amnesia), to Sacks himself, who suffers from "face blindness," a condition that renders him unable to recognize people, even relatives and, sometimes, himself (he once confused a stranger's face in a window with his own reflection), Sacks finds fascination in the strange workings of the human mind. Written with his trademark insight, compassion, and humor, these seven new tales once again make the obscure and arcane absolutely absorbing. (Oct.) (c) Copyright PWxyz, LLC. All rights reserved.


Review by Library Journal Review

Neurologist Sacks (www.oliversacks.com), who in Musicophila (2007) explored the human sense of hearing, once again mines his practice for fascinating case studies, this time to explore another sense, that of sight. In discussing the experiences of six individuals whose vision-related maladies force creative and often astonishing coping and adaptive behaviors, he talks of patients' inability to recognize faces, their late acquisition and loss of three-dimensional vision, and more. Sacks introduces each story, which is then read matter-of-factly by actor Richard Davidson. Sacks poignantly reads the chapter titled "Persistence of Vision"-about his own gradual loss of vision in one eye as the result of ocular cancer. A strong choice for nonfiction collections. ["The author's well-known style creatively balances complex medical discussion.with solid, down-to-earth prose," read the review of the New York Times best-selling Knopf hc, LJ 10/1/10.-Ed.]-Kristen L. Smith, Loras Coll. Lib., Dubuque, IA (c) Copyright 2011. Library Journals LLC, a wholly owned subsidiary of Media Source, Inc. No redistribution permitted.

(c) Copyright Library Journals LLC, a wholly owned subsidiary of Media Source, Inc. No redistribution permitted.
Review by Kirkus Book Review

Sacks (Neurology and Psychiatry/Columbia Univ.; Musicophilia: Tales of Music and the Brain, 2007, etc.) once again uses the experiences shared with him by patients and others to probe "the complex workings of the brain and its astounding ability to adapt and overcome disability."The author provides six case histories of patients with intriguing vision problems, beginning with the story of a 67-year-old concert pianist who consulted him over her loss of the ability to read musicalthough she could still perform it brilliantly from memory, and even transpose a Haydn string quartet piece which she played on the piano. She also suffered from increasing spatial disorientation and difficulty recognizing everyday items. MRI tests showed increasing neurologic damage, but this did not lessen her keen insight into her own condition, even though her ability to manage independently declined. In "Face-Blind," Sacks examines his own congenital difficulty"trouble with faces and places"which remains a problem for him at age 76. He even once confused the face of a man seen through a window with a supposed mirror image of his own faceboth sported heavy beards. The author compares his adult experience losing stereoscopic vision after suffering a tumor in one eye to that of a previously cross-eyed woman who gained it after a correction allowed her to focus both eyes. Both described a flattened perception of depth when using only one eye. Similarly, Sacks ponders the ability of the blind to visualize scenes that are described to them in vivid detail. "If there is indeed a fundamental difference between experience and description," he writes, "between direct and mediated knowledge of the world, how is it that language can be so powerful?"As usual with Sacks, an absorbing attempt to unravel the complexities of the human mind.]] Copyright Kirkus Reviews, used with permission.

Copyright (c) Kirkus Reviews, used with permission.

Sight Reading In January of 1999, I received the following letter: Dear Dr. Sacks, My (very unusual) problem, in one sentence, and in non-medical terms, is: I can't read. I can't read music, or anything else. In the ophthalmologist's office, I can read the individual letters on the eye chart down to the last line. But I cannot read words, and music gives me the same problem. I have struggled with this for years, have been to the best doctors, and no one has been able to help. I would be ever so happy and grateful if you could find the time to see me. Sincerely yours, Lilian Kallir I phoned Mrs. Kallir-this seemed to be the thing to do, although I normally would have written back-because although she apparently had no difficulty writing a letter, she had said that she could not read at all. I spoke to her and arranged to see her at the neurology clinic where I worked. Mrs. Kallir came to the clinic soon afterward-a cultivated, vivacious sixty-seven-year-old woman with a strong Prague accent-and related her story to me in much more detail. She was a pianist, she said; indeed, I knew her by name, as a brilliant interpreter of Chopin and Mozart (she had given her first public concert at the age of four, and Gary Graffman, the celebrated pianist, called her "one of the most naturally musical people I've ever known"). The first intimation of anything wrong, she said, had come during a concert in 1991. She was performing Mozart piano concertos, and there was a last-minute change in the program, from the Nineteenth Piano Concerto to the Twenty-first. But when she flipped open the score of the Twenty-first, she found it, to her bewilderment, completely unintelligible. Although she saw the staves, the lines, the individual notes sharp and clear, none of it seemed to hang together, to make sense. She thought the difficulty must have something to do with her eyes. But she went on to perform the concerto flawlessly from memory, and dismissed the strange incident as "one of those things." Several months later, the problem recurred, and her ability to read musical scores began to fluctuate. If she was tired or ill, she could hardly read them at all, though when she was fresh, her sight-reading was as swift and easy as ever. But in general the problem worsened, and though she continued to teach, to record, and to give concerts around the world, she depended increasingly on her musical memory and her extensive repertoire, since it was now becoming impossible for her to learn new music by sight. "I used to be a fantastic sight reader," she said, "easily able to play a Mozart concerto by sight, and now I can't." Occasionally at concerts she experienced lapses of memory, though Lilian (as she asked me to call her) was adept at improvising and could usually cover these. When she was at ease, with friends or students, her playing seemed as good as ever. So, through inertia, or fear, or a sort of adjustment, it was possible for her to overlook her peculiar problems in reading music, for she had no other visual problems, and her memory and ingenuity still allowed her a full musical life. In 1994, three years or so after she had first noticed problems reading music, Lilian started to have problems with reading words. Here again, there were good days and bad, and even times when her ability to read seemed to change from moment to moment: a sentence would look strange, unintelligible at first; then suddenly it would look fine, and she would have no difficulty reading it. Her ability to write, however, was quite unaffected, and she continued to maintain a large correspondence with former students and colleagues scattered throughout the world, though she depended increasingly on her husband to read the letters she received, and even to reread her own. Pure alexia, unaccompanied by any difficulty in writing ("alexia sine agraphia") is not that uncommon, although it usually comes on suddenly, following a stroke or other brain injury. Less often, alexia develops gradually, as a consequence of a degenerative disease such as Alzheimer's. But Lilian was the first person I had encountered whose alexia manifested first with musical notation, a musical alexia. By 1995 Lilian was beginning to develop additional visual problems. She noticed that she tended to "miss" objects to the right, and, after some minor mishaps, she decided that she had best give up driving. She had sometimes wondered whether her strange problem with reading might be neurological rather than ophthalmological in origin. "How can I recognize individual letters, even the tiny ones on the bottom line of the eye doctor's chart, and yet be unable to read?" she wondered. Then, in 1996, she started to make occasional embarrassing mistakes, such as failing to recognize old friends, and she found herself thinking of a case history of mine she had read years before, entitled "The Man Who Mistook His Wife for a Hat," about a man with visual agnosia. She had chuckled when she had first read it, but now she started to wonder whether her own difficulties might be eerily similar in nature. Finally, five years or more after her original symptoms, she was referred to a university neurology department for a full workup. Given a battery of neuropsychological tests-tests of visual perception, of memory, of verbal fluency, etc.-Lilian did particularly badly in the recognition of drawings: she called a violin a banjo, a glove a statue, a razor a pen, and pliers a banana. (Asked to write a sentence, she wrote, "This is ridiculous.") She had a fluctuating lack of awareness, or "inattention," to the right, and very poor facial recognition (measured by recognition of photographs of famous public figures). She could read, but only slowly, letter by letter. She would read a "C," an "A," a "T," and then, laboriously, "cat," without recognizing the word as a whole. Yet if she was shown words too quickly to decipher in this way, she could sometimes correctly sort them into general categories, such as "living" or "nonliving," even though she had no conscious idea of their meaning. In contrast to these severe visual problems, her speech comprehension, repetition, and verbal fluency were all normal. An MRI of her brain was also normal, but when a PET scan was performed-this can detect slight changes in the metabolism of different brain areas, even when they appear anatomically normal-Lilian was found to have diminished metabolic activity in the posterior part of the brain, the visual cortex. This was more marked on the left side. Noting the gradual spread of difficulties in visual recognition-first of music, then of words, then of faces and objects-her neurologists felt she must have a degenerative condition, at present confined to the posterior parts of the brain. This would probably continue to worsen, though very slowly. The underlying disease was not treatable in any radical sense, but her neurologists suggested that she might benefit from certain strategies: "guessing" words, for example, even when she could not read them in the ordinary way (for it was clear that she still possessed some mechanism that allowed unconscious or preconscious recognition of words). And they suggested that she might also use a deliberate, hyperconscious inspection of objects and faces, making particular note of their distinctive features, so that these could be identified in future encounters, even if her normal "automatic" powers of recognition were impaired. In the three years or so that had elapsed between this neurological exam and her first visit to me, Lilian told me, she had continued to perform, though not as well, and not as frequently. She found her repertoire diminishing, because she could no longer check even familiar scores by vision. "My memory was no longer fed," she remarked. Fed visually, she meant-for she felt that her auditory memory, her auditory orientation, had increased, so that she could now, to a much larger degree than before, learn and reproduce a piece by ear. She could not only play a piece in this way (sometimes after only a single hearing); she could rearrange it in her mind. Nonetheless, there was, on balance, a shrinkage of her repertoire, and she began to avoid giving public concerts. She continued to play in more informal settings and to teach master classes at the music school. Handing me the neurological report from 1996, she commented, "The doctors all say, 'Posterior cortical atrophy of the left hemisphere, very atypical,' and then they smile apologetically-but there's nothing they can do." When I examined Lilian, I found that she had no problem matching colors or shapes, or recognizing movement or depth. But she showed gross problems in other areas. She was unable now to recognize individual letters or numerals (even though she still had no difficulty writing complete sentences). She had, too, a more general visual agnosia, and when I presented her with pictures to identify, it was difficult for her even to recognize pictures as pictures-she would sometimes look at a column of print or a white margin, thinking it was the picture I was quizzing her about. Of one such picture, she said, "I see a V, very elegant-two little dots here, then an oval, with little white dots in between. I don't know what it's supposed to be." When I told her it was a helicopter, she laughed, embarrassed. (The V was a sling; the helicopter was unloading food supplies for refugees. The two little dots were wheels, the oval the helicopter's body.) Thus she was now seeing only individual features of an object or picture, failing to synthesize them, to see them as a whole, much less to interpret them correctly. Shown a photograph of a face, she could perceive that the person was wearing glasses, nothing else. When I asked if she could see clearly, she said, "It's not a blur, it's a mush"-a mush consisting of clear, fine, sharp but unintelligible shapes and details. Looking at the drawings in a standard neurological test booklet, she said of a pencil, "Could be so many things. Could be a violin . . . a pen." A house, however, she immediately recognized. Regarding a whistle, she said, "I have no idea." Shown a drawing of scissors, she looked steadfastly at the wrong place, at the white paper below the drawing. Was Lilian's difficulty in recognizing drawings due simply to their "sketchiness," their two-dimensionality, their poverty of information? Or did it reflect a higher-order difficulty with the perception of representation as such? Would she do better with real objects? When I asked Lilian how she felt about herself and her situation, she said, "I think I am dealing with it very well, most of the time . . . knowing it is not getting better, but only slowly worse. I've stopped seeing neurologists. I always hear the same thing. . . . But I am a very resilient person. I don't tell my friends. I don't want to burden them, and my little story is not very promising. A dead end. . . . I have a good sense of humor. And that's it, in a nutshell. It is depressing, when I think of it- frustrations daily. But I have many good days and years ahead." After Lilian left, I was unable to find my medical bag-a black bag with some similarities (I now remembered) to one of the several bags she had brought. Going home in the taxi, she realized that she had taken the wrong bag when she saw a red-tipped object sticking out of it (my long, red-tipped reflex hammer). It had attracted her attention, by its color and shape, when she saw it on my desk, and now she realized her mistake. Returning, breathless and apologetic, to the clinic, she said, "I am the woman who mistook the doctor's bag for her handbag." Lilian had done so badly on the formal tests of visual recognition that I had difficulty imagining how she managed in daily life. How did she recognize a taxi, for example? How could she recognize her own home? How could she shop, as she told me she did, or recognize foods and serve them on a table? All this and much more-an active social life, traveling, going to concerts, and teaching-she did by herself when her husband, who was also a musician, went to Europe for weeks at a time. I could get no idea of how she accomplished this from seeing her dismal performance in the artificial, impoverished atmosphere of a neurology clinic. I had to see her in her own familiar surroundings. The following month, I visited Lilian at home, home being a pleasant apartment in upper Manhattan where she and her husband had lived for more than forty years. Claude was a charming, genial man about the same age as his wife. They had met as music students at Tanglewood nearly fifty years earlier and had pursued their musical careers in tandem, often performing on stage together. The apartment had a friendly, cultured atmosphere, with a grand piano, a great many books, photographs of their daughter and of friends and family, abstract, modernist paintings on the wall, and mementos of their trips on every available surface. It was crowded-rich in personal history and significance, I imagined, but a nightmare, a complete chaos, for someone with visual agnosia. This, at least, was my first thought as I entered, negotiating my way between tables full of knickknacks. But Lilian had no difficulty with the clutter and threaded her way confidently through the obstacles. Since she had had such difficulty on the drawing-recognition test, I had brought a number of solid objects with me, wondering if she would do better with these. I started with some fruit and vegetables I had just bought, and here Lilian did surprisingly well. She instantly identified "a beautiful red pepper," recognizing it from across the room; a banana, too. She was momentarily uncertain whether the third object was an apple or a tomato, though she soon decided, correctly, on the former. When I showed her a small plastic model of a wolf (I keep a variety of such objects, for perceptual testing, in my medical bag), she exclaimed, "A marvelous animal! A baby elephant, perhaps?" When I asked her to look more closely, she decided it was "a kind of dog." Lilian's relative success in naming solid objects, as opposed to drawings of them, again made me wonder whether she had a specific agnosia for representations. The recognition of representations may require a sort of learning, the grasping of a code or convention, beyond that needed for the recognition of objects. Thus, it is said, people from primitive cultures who have never been exposed to photographs may fail to recognize that they are representations of something else.  Excerpted from The Mind's Eye by Oliver Sacks All rights reserved by the original copyright owners. Excerpts are provided for display purposes only and may not be reproduced, reprinted or distributed without the written permission of the publisher.