Longlisted for the School Library Association's Information Book Award 2017 - 'Over 12' category. Brie's Granddad has always been a serious man, never without a newspaper and knowing the answer to everything. But now he keeps losing track of the conversation, and honestly, Brie doesn't really know how to speak to him. At first, Fred was annoyed that Gramps had come to live with them, it meant he had to give up his room! But then he starts to enjoy watching old films with him and spending time together... although there's the small problem of Gramps calling him Simon. Follow the stories of Brie, Fred, and other young carers as they try to understand and cope with their grandparents' dementia at all stages of the illness. Adapted from true stories, and supplemented with fun activities and discussion ideas, this book for children aged approximately 7-14 cuts to the truth of the experience of dementia and tackles stigma with a warm and open perspective.

HARD COVER EDITION------WHAT'S IT LIKE to be the only son of a widowed mother who is rapidly sinking into the opaque fog of dementia, and who lives alone half a continent away? ROBERT TELL tells this tale with compassion and humor. DEMENTIA DIARY reads like fiction and covers the fifteen year period from his father's shocking death in a department store to his mother's 92nd birthday. It is meant to be a portable support group. If you have watched helplessly as your parent, spouse or friend's identity disappeared into the sinkhole of Alzheimer's Disease (or another dementia), this heart-wrenching memoir will touch you deeply

In 2009, my wife of over fifty-eight years was diagnosed with dementia with Alzheimers symptoms. My caregiving responsibilities began before that time and continued until her death in January 2018. She was provided care in her own home. As time went by, the caregiver duties became more and more demanding. It was truly twenty-four hours each day and seven days each week. My sweetheart was referred to the hospice program as a patient beginning in 2013 with a life expectancy of six months or less. At the time of her passing, she had been a hospice patient for four years, eleven months, and five days. The Diary of a Caregiver begins with her entry into the hospice program and continues until her death. Caregiving can be very frustrating at times as one never knows what to expect or when to expect it. The Diary of a Caregiver identifies many of the problems and frustrations associated with care of a dementia patient. It also identifies different techniques and solutions to some of those problems. It should be of interest to anyone who is involved in caregiving, especially those who are just beginning.

Another Cup of Tea is a book for anyone caring for someone with dementia or Alzheimer's disease. Selected from the diary of a son caring for his Mum in the latter stages of her struggle with vascular dementia. Written often in the midst of long, challenging days and nights. You'll find yourself either laughing, crying or even nodding along in recognition at the ups and downs of their time together. You'll notice how tea often saved the day, how they coped or didn't and perhaps imagine yourself in their shoes, wondering what could happen next and how you'd cope in similar circumstances. As suggested in the foreword, grab Another Cup of Tea and enjoy! Profits from book sales will be shared between Alzheimer's and dementia charities.

The true happenings of the time in the life of Nellie May born in April. A little joke we shared with Nellie regarding when she was born. Nellie did not have a happy childhood with a dad who beat her, she went through traumatic times when she had to go in the air raid shelter during the war when she was growing up. She went to a comprehensive school and started work at the age of 14. When Nellie was in her fifties, she liked to have a drink. I remember one day a taxi driver came to our house and asked if Nellie was at home I said no, he said I think I have her in my car (and he had). Looking back, we had some very funny times. Nellie was the life and soul of the party. She was feisty, head strong, not afraid to speak her mind, funny, loving, caring and beautiful she would do anything for anyone. She loved to dance and sing and play the organ. Nellie was in her eighties when she developed the terrible disease dementia, of which these diaries are about to tell. There were sad times but also some happy times. Nellie would always pronounce the word baby as babby as that is how she would say it. These diaries tell of what happened during her time with dementia.

Poetry is an engaging and inclusive activity for older people that can help develop memory, imagination and identity. This book provides guidance on setting up and monitoring poetry projects for people living with dementia in group care homes and individual families. It explains the benefits of creative expression for people with dementia, and shows how to facilitate poetry reading and writing groups in different environments. Specific techniques for introducing poetry to older people can be employed by family members or professional care staff to enhance the wellbeing of the individual living with dementia. The ethical issues of running poetry projects in dementia care are explored along with examples of poetry produced by individuals and groups, interviews with care workers, and case studies.

This open access book explores the expectations surrounding dementia, what it ‘looks like’ and how people have been treated by others. It aims to raise awareness of the different types of dementia, and how they impact the brain, body, and lived experience, including experience of Alzheimer’s disease, Vascular Dementia, Posterior Cortical Atrophy, Frontotemporal Dementia, Semantic Dementia, and Lewy Body Dementia. The co-authors reflect on their experience with informal and formal care, before finishing with a focus on the spectrum of dementia research from clinical trials to user-led research. Throughout the book, co-authors have shared personal stories of how dementia has affected them and people with lived experience of dementia share what they wish people knew about living with the disease. Co-produced by people with lived experience of dementia, academics and health care professionals, this book is an accessible resource about dementia from the perspective of people actively involved in the field and essential reading for healthcare professionals wishing to learn more about the experience of this neuroprogressive condition, as well as policymakers, and members of the public.