Dementia Friendly Worship

Religious faith is a powerful source of comfort and support for individuals and families facing dementia. Many faith leaders need help in adapting their ministries to address the worship/spiritual needs of this group. A product of Faith United Against Alzheimer's, this handbook by 45 different authors represents diverse faith traditions, including Christianity, Islam, Judaism, Sikhism, Buddhism and Native American. It provides practical help in developing services and creating dementia friendly faith communities. It gives an understanding of the cognitive, communicative and physical abilities of people with dementia and shows what chaplains, clergy and lay persons can do to engage them through worship. Included are several articles by persons living with dementia.

Each year in the UK, 225,000 people are diagnosed with dementia. The implications for aging church congregations, and for the Christian mission to people throughout their lives, are considerable. God In Fragments aims to equip those engaged in or preparing for ministry to people with dementia. It explores the theological and spiritual challenges of dementia, suggests practical ways to help those living with dementia participate in worship, and offers a wide range of prayers and worship outlines. • Part One offers theological reflection on living with dementia, spiritual awareness, creating dementia-friendly churches and accessible worship. • Part Two contains services, prayers, readings and activities suitable for those with dementia, for use in formal or informal church contexts, church cafés, care homes and hospitals. In an Afterword, Samuel Wells reflects on unlocking the gates of memory.

Churches have a vital role in helping people with dementia and their caregivers, and much to learn from them too. Cail pairs poignant stories with strategies, lesson plans, and advice for ministries that compliment community needs and church resources. Readers will find here tools for preparing their congregations to engage this important work.

Participatory Case Study Work shows academic co-researchers how to adapt and implement their methods so that data collection and analysis is authentically participatory. At the heart of this text is advocating a participatory approach to case study work, with co-construction as a catalyst for shared understanding and action in advancing ageing studies. Whilst case study research has a relatively long tradition in the canon of research methodologies, little attention has so far been paid to the importance and value of participatory case study work. This is surprising as its egalitarian and democratic value-base naturally lends itself to the co-production and co-creation of personal and collective theory drawn directly from lived experience. The book brings together over 15 years’ worth of participatory case study work in ageing studies in which the editors have been actively involved as either front-line researchers or as supervisors to PhD and MPhil studies adopting the methodology, and from where each of the contributors is selected. Real-life case examples are shared in the main chapters of the book and they provide direction as to how learning can be applied to other settings. The chapters also contain key references and recommended reading. This volume will appeal to undergraduate and postgraduate students as well as postdoctoral researchers interested in fields such as research methods, qualitative methods, ageing studies and mental health studies.

Bridging the Family Care Gap explores expected future shortages of family caregivers of older persons and identifies potential solutions. The book examines the sustainability and availability of care management models and whether they can be effectively scaled up to meet community needs. It identifies newly emerging policy initiatives at local, state, and federal levels. The book addresses the state of family caregiving science, dissemination and implementation of promising programs and supports, technological innovations, and other strategies to offset the family care gap. This edited volume also explores lay healthcare workers as guides, interpreters, and advocates in healthcare systems that provide continuity of contact for family caregivers. Details threats to family caregiving-sociodemographic, chronic disease, and socioeconomic challenges Presents solutions to the caregiving gap in a systematic, synthesized manner Addresses the intersection of family caregiving and technology Discusses chronic disease management to offset and reduce the need for family caregiving Describes models of caregiver support in work settings Reimagines the delivery of long-term services and supports with novel initiatives

This volume seeks to instigate a discussion about dementia in theatre. The discussions in this book borrow from the literature on dementia’s representation in other artforms, while reflecting on theatre’s unique capacity to incorporate multiple artforms in a live context (hypermediacy). The author examines constructions of diegesis and the use of various performance tools, including physical theatre, puppetry, and postdramatic performance. She discusses stage representations of interior experiences of dementia; selfhood in dementia; the demarcation of those with dementia from those without; endings, erasure, and the pursuit of catharsis; placelessness and disruptions of traditional dramatic constructions of time; and ultimately, performances creatively led by people with dementia. The book traces patterns of narrativisation on the stage—including common dramaturgical forms, settings, and character relationships—as well as examples that transcend mainstream representation. This book is important reading for theatre and performance students, scholars, and practitioners, as well as cultural studies writers engaged in research about narratives of dementia.

This book is for caregivers who have a desire not only to hone their caring skills, but also to deepen their relationship with God through their care. It explores feelings of loss and challenge, but turns always towards potential and hope. THESE ARE THE FACTS: There are over 100 types of dementia affecting over 50 million people around the world. But if you’re picking up this book, you probably already know that. Unfortunately, knowing the hard numbers doesn’t make caregiving less demanding, challenging, exhausting, and, yes, many times and in many ways, potentially uplifting. Caregiving is typically understood as an activity, as something we do – likely because caregivers do a lot. But caregiving is deeper than what we do. It is more than a series of tasks. It is, first and foremost, a call to love. In How the Light Shines each chapter engages an issue raised by caregivers themselves and is filled with real-life stories that convey the realities of caregiving, as well as tips and advice, and spiritual insight and guidance. It is written with both individuals and groups in mind. Each chapter includes questions and, for personal or group reflection, a spiritual practice and a prayer grounded in the pain and possibilities of it all.