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Review
“Heartbreaking but never sentimental, Williams-Paisley’s book offers an intimate look at a family’s struggle with a life-altering disease. It is also a daughter’s tribute to the mother whose disease offered her a new opportunity to ‘love unconditionally…and practice being comfortable with…[the] uncomfortable.’ A simply told, moving memoir.”—Kirkus Reviews“Kimberly Williams-Paisley has written a book that is both heartbreaking and essential. I loved it for all the love it contained but also for the wealth of practical information. The Williams family went down a hard road with dementia, and we can all benefit from their experience.”—Ann Patchett, New York Times bestselling author of Bel Canto and State of Wonder “The relationship between a mother and daughter is one of the most complicated and meaningful there is. Kimberly Williams-Paisley writes about her own with grace, truth, and beauty as she shares her journey back to her mother in the wake of a devastating illness.”—Brooke Shields, New York Times bestselling author of There Was a Little Girl “Kim’s story really resonated with me, as it will with countless others. Her beautiful, heartfelt book is an absolute must-read for mothers, daughters, and anyone dealing with a loved one living with dementia. It will also help to bring comfort to families facing any type of life-altering situation.”—Robin Roberts, Good Morning America“Where the Light Gets In is simply wonderful . . . and sad . . . and brave. This book will bring comfort to families who are experiencing the complex and confusing journey of progressive dementia while still celebrating moments of true joy. Williams-Paisley’s narrative and the resource section will help people know they are not alone.”—Angela Timashenka Geiger, Chief Strategy Officer, Alzheimer's Assocation “Generous, human, and healing; that’s what this book is. Kimberly Williams-Paisley has invited us into her life and her family so that we may know ourselves better. By sharing her story with such vulnerability and honesty, she makes it accessible to everyone, with or without a personal connection to dementia. Through it, I had the experience of seeing my own family differently, understanding my desire to love more, and connecting deeply to my own stories of illness, grief, compassion, empathy, and redemption.”—Connie Britton, Actress“Where the Light Gets In left an indelible mark on my heart. The story of love and acceptance and the unbreakable bond of family, this book will be a comfort to so many families who are going through what Kim’s went through and will be a much-needed source of strength for all those who read it.”—Sheryl Crow, Musician“Informative, relatable, and heartbreaking, Where the Light Gets In is a must-read for those who have a loved one struggling with dementia.”—Seth Meyers, Host of Late Night with Seth Meyers“Kimberly Williams-Paisley’s experience with her mother’s dementia is very moving, and you’ll be touched by so much in this book. This topic needs national attention, and Where the Light Gets Inhelps bring focus to that need.”—William Shatner, Actor"In Where the Light Gets In, Kimberly Williams-Paisley shares the brutal emotional toll that dementia takes on a family, bravely revealing the denial, the missteps, the losses, the grief. Thankfully, she also shares the lessons--how to get comfortable being uncomfortable, how to connect with her mother where she is, how to love unconditionally. Intimate, honest, and beautifully written, this book will be a tremendous resource for anyone affected by dementia."—Lisa Genova, New York Times bestselling author of Still Alice"Kimberly Williams-Paisley’s honest and heart-wrenching memoir draws a stark picture of the devastation of dementia on a family and captures the sense of injustice when the parent/child role is reversed far too young. Kimberly shares her story to honor her mother, but she galvanizes us to find a cure for a disease that slowly erases the ones we love most."—Lee Woodruff, journalist and New York Times bestselling coauthor of In An Instant
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About the Author
Kimberly Williams-Paisley is an actress, writer and advocate for dementia research and caregivers. She and her husband live in Tennessee with their two sons and two dogs. This is her first book.
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Product details
Hardcover: 272 pages
Publisher: Crown Archetype; First Edition edition (April 5, 2016)
Language: English
ISBN-10: 1101902957
ISBN-13: 978-1101902950
Product Dimensions:
5.7 x 0.8 x 8.5 inches
Shipping Weight: 11.2 ounces (View shipping rates and policies)
Average Customer Review:
4.7 out of 5 stars
249 customer reviews
Amazon Best Sellers Rank:
#68,561 in Books (See Top 100 in Books)
I am not a person that rates books but after reading this book, felt I should let others know how excellent this book is. Kimberly Williams-Paisley wrote a touching and informative book on her family's journey with her mother's dementia. There were so many moments in the book that I could relate to as I experience my own journey with my mom. I especially appreciated the reminder to love and experience my mom where she is now, not what she used to be. If you have a family member with dementia, I encourage you to read this book.
I set out to read this because I am a Fan of all that is Paisley. Very quickly the words written began to have such a simarilarty to the lost of my own Mother. We lost her after a 2 year battle of stomach cancer almost 2 years ago. Gone was the fangirl. It was replaced with the love of a new found author. One who managed to write the words that I struggle to fine or even allow myself own. She brought comfort to me and hopefully others, that have no choice but to walk this path. Bravo Kim! You made me laugh, cry and yes even manage to love your family even more.
This is an amazingly well written book, with Paisley sharing her true, unfiltered innermost thoughts and feelings as well as detailed events about her mother's diagnosis and decline. I can't believe anyone would criticize the author, calling her selfish or any other criticism. Those comments must be from those who have not gone through something similar with a parent. My mom recently died of cancer, and now my dad, who is 97% physically disabled is also developing dementia, badly. I could relate to all the thoughts and feelings she shared, in all honesty. This was a quick read, and while she never truly found a way to consistently be OK with her parent's condition and decline (nor have I), it's always helpful to read something like this just to know that someone else has gone through a similar experience and to see that they basically felt the same way about it. Kudos again to her for her honesty and also for mentioning God and spirituality here and there. I'd absolutely recommend this book to anyone who has gone through or is going through something similar with a parent.
I loved this book for so many reasons: it's candid, loving and a real look at one family's journey with dementia. My Dad was recently diagnosed with Alzheimer's and I was concerned about reading this. Would it scare me more than I already am? Would it be a dismal look at what lies ahead?The answer is yes. I am scared and realize the future isn't rosy. I mourn for what my Dad is going through and losing. This book however, gave me HOPE. Hope that we too will find 'light' wherever we can on this journey with my Dad.We will embrace whatever comes next and move forward as a family, looking for where e light shines in.Helpful resources at the end, as well.
Although I have a very busy schedule. I am having a hard time putting this book down. I was hooked from Chapter 1. It is very well written, informative and endearing. I also read Diary of a Player by Brad Paisley and thoroughly enjoyed that book too. I am almost finished with it and will be sad when it is finished. I feel that way about all the good, well written, interesting wonderful books that I read. Whether you have dementia in your family or not this book is a must read. Thank you Kimmy
As someone whose mother was diagnosed with a form of dementia (FTD) in 2016 at the age of only 61, it has been a struggle for me and my family to cope with the loss of ‘old mom’ and deal with ‘new mom’. This book was a breath of fresh air – knowing we aren’t alone in our thoughts & feelings and struggles with this terrible disease. I’ve adored Kimberly Williams-Paisley as an actress and was shocked to hear about her families struggle with this awful disease as well. I adored every page of this book, laughed and cried along with them all. I appreciated the little nuggets of wisdom from their journey & will try and embrace every one of them with our own journey. “Instead of wishing for things to be different, choose to embrace the life in front of you.â€â€œI need to love my mother in the innocent way my children do. The empathetic way Mom herself has loved people, sometimes total strangers, her whole life. I need to see her as she is, instead of how I want her to be.â€â€œRing the bells that still can ring. Forget your perfect offering. There is a crack in everything. That’s how the light gets in.â€
My mom also has ppa, so I was really curious to see how others dealt with their mother having this disease. I first read it at the library and as soon as I finished it I went and bought it. I cried throughout the whole book, but mostly out of relief that someone else has the same emotions and problems that I had. Kimberly was so honest with the trials that she went through with her mother and father, and it was a relief knowing that my family wasn't the only one going through this. Many times while I was reading I just wanted to talk to Kimberly and compare stories. If you have a family member with dementia, I highly recommend that you read this. Some parts are hard to read, but it's not an easy disease. Thanks to Kimberly for sharing her experience and wisdoms to others.
This book was so honest about what a family faces with the diagnosis of a parent with dementia, in any form. I found myself recognizing so many of the things that the Williams family have experienced, and that brings comfort to me...I'm not alone. I wept at some of the familiar stories that I'd already lived with my mother's diagnosis and living as the secondary caregiver, following my Dad. Thank you, Kim, for sharing your story. It gives hope and peace to those who are in a very similar situation. God bless you and your family.
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