Description
- Getting a specific diagnosis is crucial. You should understand how your loved one's brain changes with dementia.
- Taking care of yourself is not optional; it's mandatory. It will make you a better care partner. It's not selfish, it's self-preserving.
- You don't have a choice about being on this dementia caregiving journey. But you do have a choice in terms of how you approach it and reframe it.
- Caregivers are human. You aren't always patient and selfless, you have challenges and struggle with conflicting emotions--and that's okay.
Ultimately, The Unexpected Journey shows you how to care for yourself while doing one of the hardest, most heartbreaking jobs in the world. Because if you don't take care of yourself, you are not going to be able to look after anyone else--especially your loved one with dementia. For anyone caregiving for a loved one with any form of dementia, and even for those caregiving for other conditions, The Unexpected Journey shows that you are not alone. As Emma writes, "I know that no two caregiving journeys are the same, but we are connected by the same unchosen thread. It's not an easy path for you, your loved one or your family. But I'm here to let you know that you are not alone, and, in time, you will be okay."
Author: Emma Heming Willis
Publisher: Diversified Publishing
Published: 09/09/2025
Pages: 400
Binding Type: Paperback
Weight: 0.97lbs
Size: 9.21h x 6.14w x 1.18d
ISBN13: 9798217169023
Large Print
BISAC Categories:
- Self-Help | Motivational & Inspirational
- Health & Fitness | Diseases & Conditions | Alzheimer's & Dementia
- Family & Relationships | Life Stages | General
About the Author
Emma Heming Willis is a British and Indian/West Indian model, entrepreneur, advocate, wife, and mother of two and stepmother of three. She is the co-founder and Chief Impact Officer for Make TimeWellness, and founder and CEO of CocoBaba, a vegan skincare company. Emma's husband Bruce Willis was diagnosed with frontotemporal dementia (FTD), and she has since become a powerful advocate for dementia awareness, support for the lived experience of FTD for care partners and families, and research to end FTD and all forms of neurodegenerative disease.

