If you were asked to name a terminal illness, it is likely that Alzheimer’s would not be your first choice. However, from my own perspective, when you consider that there is no cure for this horrible disease, how can it be called anything else but terminal? When someone is diagnosed with Alzheimer’s disease, a family becomes focused on learning more about the illness, how it will affect their loved one, and what kind of care will be necessary. If they have no previous exposure to Alzheimer’s with other family members or even friends, what they may fail to realize is the extent to which each member of the family will be affected by the disease.
“Helping the family face their grief and work through the accompanying emotions of sadness, anxiety, anger, guilt, and — finally — acceptance may be the most important single task of the clinician working with a member of the Alzheimer’s family.” This quote succinctly describes what author Robert B. Santulli, M.D., addresses in The Alzheimer’s Family: Helping Caregivers Cope. While the physician’s focus is on caring for the person with Alzheimer’s, the focus of a clinician is on caring for the “Alzheimer’s family.” Reading this book will help to ensure a clinician is well versed in the disease’s impact on the family.
Beginning with identifying the primary caregiver, a process in which family dynamics plays a large role, the author then identifies and elaborates on four areas of providing care for the person with Alzheimer’s (passive, active, cognitive, and behavioral). A discussion of the basics of memory loss and dementia follows, along with the impairments in activities, behavior, and cognition that typically occur with Alzheimer’s.
A listing of common medications that can lead to an impairment of short-term memory is also included, running the gamut from antidepressants to muscle relaxants to those for Parkinson’s and cardiovascular disease. Current medications illustrate one more factor a physician must take into consideration when trying to determine if the memory loss is due to a form of dementia or one of the medications the person may be taking.
One chapter deals specifically with mood and behavioral issues of the person with Alzheimer’s and includes aggressiveness, apathy, agitation, and depression, along with several others. The last line in each of the subchapters refers to a discussion in the appendix on medications for that particular challenge.
Santulli states that the purpose of the book is to “prepare clinicians to become skilled counselors for the Alzheimer’s family.” In that regard, much information is indeed presented that will help a clinician support the family in the many areas of caring for their loved one. Given the book’s subtitle, Helping Caregivers Cope, I was surprised that the shortest chapter in the book is titled “Caregiver Stress.” I suppose that one can define the entire family as the caregiver rather than a single person, and caregiving as the family’s handling of the myriad tasks and emotions involved in the journey upon which they embark after diagnosis. As presented in an earlier chapter, to minimize any resentment and anger that may surface in an individual caring for a loved one with Alzheimer’s disease – which one would assume is responsible for a great deal of stress – the author advises “Blame the disease, not the person.”
One particularly helpful section in a chapter on maintaining a connection with the family member who has Alzheimer’s disease is a list of “do’s” and “don’ts” when communicating with them. In fact, it seems each item on the list aims to preserve any remaining cognition they may have of themselves by working with their deficits instead of calling attention to them. As such, these lists may be the most valuable references family members can have regardless of whether a clinician is involved. Although it is certain clinicians will find The Alzheimer’s Family valuable, it can be a beneficial resource for the family as well.
Throughout this book, it is no stretch of the imagination to feel as though you are the person who has been diagnosed with Alzheimer’s and are reading about your own future and that of your immediate family and close friends. Rather than being frightening – which the disease is, no doubt – it is more of a play-by-play book from diagnosis to treatment to the end of life. If you have personal experience with a family member who has Alzheimer’s, or has died from the disease, you may well find yourself grieving for their loss and yours in the last chapter, “The End of the Journey.”
“…it is important to remember that the kindest, fairest way to treat someone with Alzheimer’s disease is usually to do what will cause them the least distress.” If a clinician gleans nothing else from reading The Alzheimer’s Family but this simple prescription for care, they will provide a great service to a family by using it as a preface to each step along the way in caring for the family as a whole.
The Alzheimer’s Family: Helping Caregivers Cope
W. W. Norton & Company: October 31, 2011
Hardcover, 256 pages
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Klein, T. (2011). The Alzheimer’s Family: Helping Caregivers Cope. Psych Central. Retrieved on January 25, 2015, from http://psychcentral.com/lib/the-alzheimers-family-helping-caregivers-cope/00010270
Last reviewed: By John M. Grohol, Psy.D. on 30 Jan 2013
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