Caring for elderly parents is challenging. It’s a season of life that requires grace and strength that can only come from God. In The Caregiving Season, Jane Daly shares personal caregiving stories, offering practical advice to help you honor your aging parents well and deepen your personal relationship with Christ along the journey.

Realize the value and blessings of participating in mentoring relationships during all stages, ages, and seasons of life. Women often don’t think they know enough to be a mentor, or fear rejection if they ask someone to mentor them. Others don’t think they need mentoring. However, throughout the Bible, God calls spiritually younger and older women to learn from and teach one another. Mentoring for All Seasons helps answer questions like these: •What is mentoring? •How do I find a mentor? •Why does God want us to mentor one another? •What are the blessings of mentoring? Through true stories from mentors and mentees in life seasons from tween through death—along with the author’s personal experiences, helpful tips, Scriptures to study together, and biblical mentoring relationship examples—Mentoring for All Seasons encourages women to be intentional about sharing their life experiences and God’s faithfulness with other women.

Through personal experience as a caregiver to my parents, I gained first-hand knowledge of the responsibilities family caregivers carry on their shoulders. It became important for me to find out what other family caregivers say they need to help sustain their spirit during the journey of caring for someone they love. The outcome of this inquiry is a devotional developed in direct response to family caregiver interviews and their answers to survey questions. Woven between the pages of this devotional is a message for family caregivers, individuals concerned about family caregivers, faith communities, and for community groups that are not faith-based. The devotional is a companion for the caregiving journey that invites you to seek spiritual strength and wisdom from God and to replenish your spirit of compassion and love.

The US Census Bureau tells us that the retired and retiring populations are in the majority. Those born between 1945 and 1964 are now tasked with the care of the previous generation, from choosing housing to selecting final resting place. Julie-Allyson Ieron, through personal experience and extensive interviews and research, has compiled a resource that will inform as well as delight. Yes, delight! Although this can be an overwhelming time of life, it can be managed and even enjoyed. If you are the pickle in the middle of the sandwich generation, this book is for you! The Overwhelmed Woman's Guide to Aging Parents provides practical guidance on such topics as fostering independence in your parent, providing a safe environment, and advocating for your parent in addition to a comprehensive list of resources and Take Action points.

As I stand at the threshold of this book, I am acutely aware of the delicate yet profound journey we are about to embark on together. The journey of caring for aging parents is one that many of us will inevitably face, yet it remains a topic often shrouded in uncertainty and apprehension. In writing this book, my aim is not only to provide practical guidance and support but also to offer a beacon of light amidst the sometimes tumultuous waters of caregiving. Drawing upon my own experiences, as well as insights gleaned from caregivers and professionals alike, I hope to illuminate the path ahead and instill a sense of reassurance and empowerment within you, the reader. Within these pages, you will find a roadmap for navigating the complexities of aging, from understanding the physical and emotional nuances of growing older to making difficult decisions about medical care and end-of-life preferences. You will discover strategies for fostering open communication, building a support network, and maintaining your own well-being amidst the demands of caregiving. Above all, I invite you to approach this journey with an open heart and a willingness to embrace the challenges and joys that lie ahead. For in caring for our aging parents, we not only honor the love and sacrifices they have bestowed upon us but also embark on a profound journey of growth, compassion, and resilience. May this book serve as a guiding light, illuminating your path and offering solace and wisdom along the way.

Assisting someone with Alzheimer’s disease or another illness that causes dementia is incredibly demanding and stressful for the family. Like many disabling conditions, Alzheimer’s disease leads to difficulty or inability to carry out common activities of daily life, and so family members take over a variety of tasks ranging from managing the person’s finances to helping with intimate activities such as bathing and dressing. Key coverage in Caregiving for Alzheimer’s Disease and Related Disorders includes: Early diagnosis and family dynamics Emotional needs of caregivers Developmentally appropriate long-term care for people with Alzheimer’s Family caregivers as members of the Alzheimer’s treatment Team Legal and ethical issues for caregivers Faith and spirituality The economics of caring for individuals with Alzheimer’s disease Cultural, racial, ethnic, and socioeconomic issues of minority caregivers Advances in Alzheimer’s disease research Caregiving for Alzheimer’s Disease and Related Disorders offers a wealth of insights and ideas for researchers, practitioners, and graduate students across the caregiving fields, including psychology, social work, public health, geriatrics and gerontology, and medicine as well as public and education policy makers.

Caring for people with disabilities often becomes an all-encompassing responsibility for one or more family members. To manage the multifaceted demands, caregivers must possess strong multitasking skills, including the ability to assist with daily life tasks; provide emotional support; help with financial affairs; mediate and advocate with health care providers. Maintaining balance within their own lives can become incredibly challenging for caregivers. More often than not, providing care for family members or loved ones occurs at the expense of the caregivers’ well-being. And for caregivers who themselves have disabilities, it further complicates matters. Multiple Dimensions of Caregiving and Disability addresses concerns that have been long familiar to the caregiver population and examines the current state of family care for individuals with disabilities. With a lifespan perspective, this concise reference reviews the literature on specific problems of caregivers and explores which care strategies are effective, promising, or lacking in available resources and support interventions. Contributors also explore the more fluid and subjective aspects of caregiving, such as feelings, spirituality, and family roles. Suggestions for future policy improvements, particularly within the public health sector, are discussed as well. Topics covered include: • Family dynamics and caregiving for people with disabilities. • Parent caregiving of children with disabilities. • Race, ethnicity, socioeconomic status, and caregiving. • Educational, training, and support programs for caregivers. • Emerging technologies to aid caregivers. • Developing partnerships between caregivers and health care providers. Multiple Dimensions of Caregiving and Disability is a must-have resource for researchers, scientist-practitioners, policy makers, and graduate students across such disciplines as clinical psychology, nursing, social work, public health, medicine, and social and education policy.

As people live longer and health care costs continue to rise and fewer doctors choose to specialize in geriatrics, how prepared is the United States to care for its sick and elderly? According to veteran psychologist Seymour Sarason’s eloquent and compelling new book, the answer is: inadequately at best. And rarely discussed among the grim statistics is the psychosocial price paid by nursing home patients, from loneliness and isolation to depression and dependency. In Centers for Ending, Dr. Sarason uses his firsthand experience as both practitioner and patient in senior facilities to reveal wide-ranging professional and moral issues affecting this seemingly familiar terrain. Insensitive medical personnel, poorly trained nurses and aides, indifferent administrators, and a prevailing culture content with treating “bodies” instead of human beings are identified as contributing factors. Drawing on America’s rich history of large-scale solutions to social problems, Dr. Sarason offers penetrating insights and bold suggestions in such areas as: The widening care gap between haves and have-nots. Why professional caregivers fail to understand patients. The nursing home resident as immigrant. Why previous reform efforts have not worked. The need for a Presidential commission for the elderly. The scenario if conditions are allowed to remain as they are or worsen. This concise volume is essential reading for researchers, graduate students, professionals, practitioners, and policy makers across such fields as geriatric medicine, health psychology, social work, public health, and public policy. Centers for Ending is a clarion call to be ignored at great cost to our elders and ourselves.