Kondracke's moving and remarkably frank narrative chronicles his own transformation from a careerist to a caregiver and disease activist whose religious faith grew more profound as he tackled his wife's illness. In turn, he explores the realities of disease politics and argues for increased government investment in medical research.
©2001 Morton Kondracke; (P)2001 Books on Tape, Inc.
"A deeply personal and bracingly honest account." (Publishers Weekly)
"This book is a love letter, an involving story of the devastating impact of Parkinson's, and a polemic demanding a substantial increase in federal funds for medical research." (Booklist)
I had never heard of the author or his wife but of course have heard of MJ Fox. My wife was recently diagnosed with PD at age 43. Not knowing what the future holds this book showed me the importance of not wasting the good time we have now before the symptoms advance. Also, there may never be a cure. Twenty years ago Millie was told a cure was 5-10 years away. All they needed was money and time. Millions of dollars and 20 years later the docs still say 5 years to a cure. Hope for the best prepare for reality.
30-something nursing student obsessed with all things medical, historical and scientific....
The author relays in detail his wife's ordeal with Parkinson's... very informative, easy listen. As a healthcare worker, I enjoy hearing the patient perspective. Bonus political history of disease research funding.
Love Politics & Parkinsons
Milly ... she was a fighter for life.
This book made me think about the truth of Parkinsons and what people (our surviving loved ones) go through when caring for those stricken with the disease. This book shows true Love, & the political fight for research. How Hollywood helped with Michael J. Fox at the forefront to bring awareness.
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