My husband had Lewy body dementia (LBD). Even as a registered nurse, I had only a vague idea of what it was. From the little information I could find, I knew that the prognosis was not good. It was then that I started looking for accounts of people with that diagnosis. What was it like for them and for their caregivers? Every story I read helped me feel less alone and more informed.
Because the course of the disease is a little different for each individual, it was difficult to know what to expect next. I recorded our journey over the next five years. Writing about the highs and the lows helped me honor the process. It is my hope that by adding this story to the overall picture of LBD that others will find their journey less frightening, more purposeful, and more honorable in spite of the difficulties.
外文書商品之書封，為出版社提供之樣本。實際出貨商品，以出版社所提供之現有版本為主。部份書籍，因出版社供應狀況特殊，匯率將依實際狀況做調整。
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