This book was a very hard read for me. Not because of the writing, but because of the subject matter. I had just placed my father and his wife into a continuing care community when my book club chose this book. The stories of lost independence and the price of safety on quality of life hit me hard. After they moved in my dad went straight to Memory Care. His freedom is gone and he feels it keenly. It's true that he's safe, but I feel like I had a hand in ending his freedom. Of course in my head I know this isn't true, the circumstances were - and still are - way beyond my control, but still.
The takeaway from this book is to communicate clearly with your loved ones what you want as an end-of-life plan. Also, it's important to take an active role in choosing help and help communities. Finally, hospice is a far more humane way to treat the end-of-life experience than heroic measures and ICU. Quality of life is the most important thing and this is defined on a individual basis.