In 2009 my wife of over 59 years was diagnosed with Dementia with Alzheimer's symptoms. My care giving 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 24 hours each day and seven days each week. My Sweetheart was referred to the hospice program as a patient beginning in March 2013 with a life expectancy of six months or less. At the time of her passing, she had been a hospice patient for 4 years, 10 months and 5 days.
The Diary of a Caregiver
begins with her entry into the hospice program and continues until her death. Care giving can be very frustrating at times as one never knows what to expect or when to expect it.
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 care giving especially those who are just beginning.