Bill McNair

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Again, I was left pondering Marty’s reality, and what it meant to be dying. And the nature of ALS, and specifically, his ALS, with its cognitive impairment. No one explained that, or even talked about it. In Clinic visits, it didn’t come up—not for his perspective, or for my part in his life. I had to feel my way through it.
Dance Me to the End: Ten Months and Ten Days with ALS
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