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.
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.
My Mum was 74 when she began her Dementia journey, being firstly diagnosed with cognative memory loss, followed by an Alzheimers diagnosis. This book charts our journey through that, living together, as a family, whilst, as her carer, I walked through it at home with her until her death nearly 11 years later. She changed, I changed, we laughed, we cried, we struggled as we witnessed as a family mum's transformation from a vibrant woman to an immobile, non verbal shadow of her former self .As difficult as it was, we stayed together and we walked through it with God and with love until He called her home.
PAPERBACK & DOWNLOAD EDITIONS---For 15 years, Robert Tell was his widowed Mom's caregiver as her mind and personality disappeared into the fog of dementia. He tells the tale with compassion and humor in this full length, fast moving memoir. His lesson: Caregiver burnout can be helped. If you are watching your loved one vanish into the sinkhole of Alzheimer's Disease (or another dementia), "Dementia Diary" will lift your spirits.
Clive Beaumont was diagnosed with Younger Onset Dementia at age 45, when his children were aged just 3 and 4. He had become less and less able to do his job properly and had been made redundant from the Army the year before. Clive's wife, Helen, tells of how she and the rest of the family made it through the next six years until Clive died: the challenge of continually adapting to his progressive deterioration; having to address the legal implications of the illness; applying for benefit payments; finding nursing homes; and juggling her responsibilities as a wife, a mother and an employee. She also describes the successful founding and development of The Clive Project, a registered charity set up by Helen and others in a bid to establish support services for people with Younger Onset Dementia. Younger Onset Dementia is comparatively rare, but not that rare. This story is for the family and friends of people with the condition, for the people themselves, and for the professionals working with them.
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.
You left the doctor's surgery before you could ask the things you really wanted to know. You've googled your question about dementia and had 75 answers, all contradicting each other. You asked your best friend - but they looked at you strangely. You have so many questions, but no idea where to start finding the answers. Here they are. In this book you'll find the definitive, expert responses to all your FAQs: On Dementia. No question is too simple, too embarrassing, too rude or too offbeat to be included, and each one has been asked by thousands of people just like you. Will my partner stop loving me now they have dementia? Does my mum have to go into a home now? Is dementia a terminal illness? All these questions, and hundreds more, are covered in this short but powerful, helpful, practical guide to understanding the nature, and impact, of dementia. Read at your leisure, or dip in and out when you most need the support or to shine a light on the issues and concerns that are making you uncomfortable or unhappy, and to bring them out of the shadows so you can understand and accept them.
Afterword by Alzheimer's Research UK. 'Shobna Gulati is the Northern heroine of a nation' - Lemn Sissay 'Lucid and probing' - Guardian 'Wonderful and emotional, a masterpiece of resilience.' - Emma Kennedy Remember Me? is a memoir about caring for a parent with dementia and the memories that resurface in the process. In her first book, Shobna Gulati sets out to reclaim her mother's past after her death, and in turn, discovers a huge amount about herself and their relationship. Remember Me? captures the powerful emotions that these memories hold to both Shobna and her mother; secrets they had collectively buried and also the concealment of her mother's condition. What ensues is a story of cultural assimilation, identity and familial shame.
This story poses a profound question - do we accept the hand that fate deals us, or do we battle to make the most of the life we have and help others in the process? Chris Graham, just 38 years old but already facing the advanced stages of Alzheimer's disease, has emphatically chosen the latter. Having lived through a troubled childhood, Chris joined the British Army at a young age and found that the life of a soldier provided him with a much-needed sense of stability. However, his world was turned upside down when, at just 34 years of age, he was diagnosed with a form of early onset dementia. This brutal disease had already claimed the life of his father at 42, along with several other members of his family, and tragically had already confined his brother to a nursing home at the age of 43. In his brother's life, Chris could see a terrifying window into his own near future. Chris, though, is an extraordinary human being. Having been handed nothing less than a death sentence, he decided overnight to stand up to this horrendous disease and do something to leave his mark before it was too late. And so it was that last year, Chris embarked on an awareness-raising 16,000-mile solo cycle around North America, armed only with his bike, a sense of humour, and some good old-fashioned British grit. Leaving his ever-supportive wife Vicky and baby son Dexter at home, he took on huge challenges - for instance, the fear that the ability to discern left from right might leave him at any point while navigating an entire continent - and made it home in time for Christmas, determined to spending however long he has left pouring his love and attention into his family life. Five Minutes of Amazing is both the story of Chris' epic journey and of his fight against the disease increasingly being recognised as the defining disease of our generation. Inspiring and heart-rending in equal measure, it's as important as it is moving, and it will touch everyone who reads it.
Providing key messages for practice, they outline a range of protection measures against "disability by association" to reduce the risk of stigma and victimisation.
