An invaluable resource for everyone concerned for the vulnerable people in their lives. Estimates suggest almost half of the adult population will someday be a caregiver, whether for an aging parent, an ailing partner, or a disabled family member. It is a role that tends to fall on people without warning, and almost certainly without preparation or training. Even Dr. Kimberly Fraser, a nurse who ran a large home support business, found it a struggle when her father and husband needed increasing levels of care. In this timely and urgently needed book, she gives readers sound, practical advice on how to meet with humanity and optimism the bewildering array of challenges facing where to find help, how to navigate a confusing healthcare system, how to deal with constant demands, how to keep one’s own life from being overwhelmed by new responsibilities. Based on personal experience, prodigious research, and extensive interviews, The Accidental Caregiver is an invaluable resource for everyone concerned for vulnerable people in their lives and communities.
This book talks about the stressors of being in the caregiver role for a loved one or friend.
Kimberly also talks about her own experience with her dads dx of MS and her mother taking on the caregiver role.
Kimberly has worked many years in various Home Care roles.
I enjoyed this book as I think it was a good reminder as a Home Care Nurse myself that sometimes we can be so task orientated we forget to take a minute and look at the whole picture. What else could we do for this client and their caregiver to better support them.
It’s a little frustrating the parts that talk about Home Care perhaps not giving info of possible services or the care not being good. I guess I take that personal as we try to do our best but unfortunately times change and unless the government changes things our hands are tied as to what can be offered and the care given. I 100% agree we need to put services in before the caregiver feels burnt but sometimes they don’t want to take on help as it can be just as daunting. I can relate as sometimes thinking of getting different services for Emmerson to help feels like more work then the help would be.
I wish I had millions to make the perfect world for caregivers to be fully supported and the patients to also get all the care they deserve.
If you know someone who is a caregiver be their listening ear. Sometimes they just need to vent or have a quick coffee or maybe a meal dropped off. Doesn’t have to be anything extravagant. Also don’t ditch them as friends, they need you more now then ever.
The Accidental Caregiver is a thoughtful and engaging guide for anyone who finds themselves caring for a loved one at home. Dr. Fraser is passionate about her decades of work with family caregivers, and her personal experiences add both authenticity and credibility to her writing.
The families she introduces in the book are relatable and interesting and their stories are informative. The narrative aspect of the book is an effective way to illustrate the themes and bring the challenges to life. The author strikes an important balance between acknowledging the difficulties of caregiving and the burden many caregivers feel, while offering suggestions for realistic self-care and celebrating the incredible contribution they’re making to their family and community.
In addition to the stories, Dr. Fraser also shares very practical tips and advice throughout the book. Each chapter contains one or more breakout boxes that provide more detail on topics such as Finding support in your community, Using the right language to get action, Helpful record keeping, and so on.
This book would make a thoughtful gift to anyone in a family caregiving role. It would also be helpful for their extended family and friends, to help them understand the challenges faced by caregivers. As Dr. Fraser says, “It’s essential for caregivers and the family member or friend they are caring for to feel like they are part of a community.”
I received a free copy of this book in exchange for my honest review. As a caregiver for my mentally ill son, with very little support in place a lot of this didn't pertain to my situation, but I really related to the tips on self care, and on how best to support those in caregiving roles, it will help me to better support others (if y'all know me, I'm gonna drop off some nutritious and comforting soup), but also to accept help from those who offer. I appreciated the statistics, and the focus on creativity in managing the emotional strain. My rating would likely be higher if I were in a more traditional caregiving role, and if I were located in Canada it would be more helpful to me in my position in social services, but it still helped me with perspective and gaining knowledge.
This book was very informative without being overwhelming. I have been a caregiver for several people in my family and am still in a caregiving role. I related to the different stories woven throughout and found it therapeutic. There is nothing better than feeling like someone truly understands how you feel. I can understand the many frustrating scenarios these caregivers had to go through as some were similar to my own. I appreciated the tips and resources that were given. This would be a valuable resource for anyone dealing with a family or friend that needs help due to illness or a disability.
Good information reported in a no nonsense narrative. Many anecdotes from caregivers in the trenches. The only "negative" I had with the book is that it is very Canada centric. While the guidance and stories can be relatable to an US audience there is a very real difference between the way the two countries deliver medical care and services.
Powerful assemblage of accounts from caregivers who have to do this virtually alone. Highlights the agonies of caregiving and how the lack of coordination harms us all.