『Living With Brain Disease』のカバーアート

Living With Brain Disease

Stroke, Neurodegeneration, and the Changing Mind

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タイトルを¥1,429で購入し、プレミアムプランに登録する ¥1,330で会員登録し購入
期間限定:2026年5月12日(日本時間)に終了。詳細はこちら。
2026年5月12日までプレミアムプランが3か月 月額99円キャンペーン開催中。
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オーディオブックをお得な会員価格で購入できます。
会員登録は4か月目以降は月額1,500円で自動更新します。いつでも退会できます。
オーディオブック・ポッドキャスト・オリジナル作品など数十万以上の対象作品が聴き放題。
オーディオブックをお得な会員価格で購入できます。
30日間の無料体験後は月額¥1500で自動更新します。いつでも退会できます。

Living With Brain Disease

著者: Dr Elias Morton
ナレーター: Tess Stalker
タイトルを¥1,429で購入し、プレミアムプランに登録する ¥1,330で会員登録し購入

期間限定:2026年5月12日(日本時間)に終了

30日間の無料体験後は月額¥1500で自動更新します。いつでも退会できます。

¥1,900 で購入

¥1,900 で購入

今ならプレミアムプランが3カ月 月額99円

2026年5月12日まで。4か月目以降は月額1,500円で自動更新します。

概要

There is a particular kind of fear that arrives when the brain is involved. People can face heart disease, lung disease, kidney disease, and even cancer with a grim determination, but when the doctor begins to speak about the brain, something changes in the room. The atmosphere tightens. The future feels less predictable. The questions become more personal, more intimate, and often more frightening, because the brain is not only an organ that keeps us alive. It is the place where our sense of self seems to live. It holds our memories, our language, our personality, our judgement, our humour, our patience, our ability to plan, and our capacity to recognise the faces we love. When the brain is injured or begins to change, it can feel as if life itself is being rearranged from the inside out.

This audiobook is written for people living with brain disease, and for the families and friends who find themselves living with it too. It is written for the person who has had a stroke and now feels as if their body is unfamiliar. It is written for the partner who hears a loved one speak differently, hesitate over words, or lose the thread of a conversation, and wonders whether this is temporary or the beginning of something long-term. It is written for the adult child who notices slight changes in a parent’s mood, attention, or memory and feels a quiet dread they cannot easily name. It is written for the caregiver who is exhausted, guilty about feeling exhausted, and uncertain how to describe a life that has become both meaningful and unbearably heavy. It is also written for the person who has a diagnosis on paper but still feels unseen, because the world tends to recognise disability more readily when it is visible.

©2026 Deep Vision Media t/a Zentara UK (P)2026 Deep Vision Media t/a Zentara UK
アルツハイマー・認知症 心理学 心理学・心の健康 神経科学・神経心理学 身体的病い・疾患
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