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.

How to live a full and rewarding life after a dementia diagnosis. Keith Oliver was diagnosed with young onset dementia at the age of 55. Unaware at the time that dementia could affect people of this age, Keith set out to increase public awareness of the condition and dispel the myths about the illness. Using a unique diary format, this intimate and empowering memoir captures what everyday life with dementia is like, offering both a candid look at its struggles, and a profoundly moving account of Keith's journey to live a full life afterwards.

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.

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

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.

The Alzheimer’s Diaries (originally published as a blog) charts the progression of his illness, from diagnosis to the funeral. Susan dubbed the illness ‘Ms Alzheimer’s’ and describes the hateful impact on the man she loves.

Dementia not only affects the person presented with the diagnosis, but their family and friends too. This book provides practitioners with strategies to support the whole family and understand their dementia journey both pre- and post-diagnosis. This is facilitated through a series of activities and reflective prompts. There is also a dedicated chapter offering structured exercises for health and social care practitioners and students. The book introduces the Lawrence family, where Peter has been diagnosed with dementia, and provides perspectives from each family member, allowing practitioners to become acquainted with the lived experience of everyone involved. The reflective questions allow readers to become actively engaged to maximise their knowledge and understanding, and to better contextualize what the dementia experience feels like for family and friends. With its focus on the all-important lived experience of the whole family during the diagnostic process and beyond, this is essential reading for any practitioner working with people with dementia.