- Sep 15, 2010 by retirelife
A columnist and book dealer from Spring Hill Florida Gary Joseph LeBlanc offers a personal and down to earth account of his experience caring for his father who suffered from Alzheimer’s disease. This common sense account of is a must read for anyone caring for a loved one with Alzheimer’s disease. Written as a completion of sixty-five articles from his column, LeBlanc gives an encouraging and enlightening guide for anyone navigating the turbulent waters of caring for a loved one with Alzheimer’s disease.
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- Sep 1, 2010 by retirelife
By Mary Jo Garinger
My mom had been diagnosed with Alzheimer’s Disease seven years before my stepfather passed away suddenly. She had already been started on Aricept, a drug used to help alleviate some confusion in those with Alzheimer’s, but I hadn’t fully grasped the severity of her dementia and how much my step-father had cared – and covered up – for her until his passing five years ago.
As we stood at the hospital, Mom had no idea why she was there or what had happened to her husband, although I had told her repeatedly. The doctor would ask her questions and she would turn to me for the answers. She repeatedly asked me, just seconds apart, “Why are we here?” and “What’s a seizure?” when I told her how her husband had died.
My first task in taking charge of her care was to get a baseline on her medical condition, so I took her to her neurologist. She reconfirmed the Alzheimer’s diagnosis and suggested that I take her to a geriatric institute where she would receive the appropriate medical and psychological care. After she was evaluated by a full panel of medical experts, I received a written prescription stating my mother needed “24 hour assistance with medications, cooking meals, eating on a regular basis, daily hygiene, and observation for falls.” I was encouraged to seek Power of Attorney (POA) and move her to a safe environment. Convinced I was doing the right thing, I obtained the necessary medical signatures and paperwork so I could legally make medical and financial decisions for her.
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- Aug 26, 2010 by libbymullen
All this week we are taking a look at what the five essential questions to ask when evaluating an assisted living facility are. Today, we address question number four:
What is the culture like?
Of all the responses we received when asking what the most important questions were, the most common response was FOOD! Your parents have been cooking for themselves for decades, and have their own tastes and thoughts on how things should be prepared. Oftentimes, the food made at ALFs is mass-produced, with many dietary concerns in mind (low salt and low sugar content are the most common features – and bring on the largest number of complaints). Ask the facility for a copy of a recent weekly or monthly menu. Is there much variety? Are there more than one option at every meal? If the resident decides they don’t want to eat that night’s fare, is there a kitchenette in their apartment or on their floor that they can use instead? Sometimes, facilities will keep a dress code for their cafeteria – does your mother prefer the comfort of a nightgown to a skirt and blouse?
In the other homes your parents’ have chosen throughout the years, they probably only considered how their own family would interact within its walls. Now, however, they will have new housemates. During your visit, does it seem like the other residents interact with each other friendly and frequently, or are they all holed up in their rooms? Which environment would your parent be more likely to prefer? Of course, friendly staffers are always an advantage. Do they make an effort to chat with the residents about their day, or is it strictly business?
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- Aug 24, 2010 by retirelife
By Joan Wright
As I sat in the back of the room, listening to the stories of caregivers about whom I was to write an article, I realized to my surprise that they were talking about me! Not me, specifically, but the role I had been playing without even realizing I was – the role of a caregiver. I, too, could recall countless trips escorting my parents to and from an assortment of doctors’ appointments, trying to coordinate medications and dietary needs, assisting with household duties that became more cumbersome for them, and becoming the designated driver for trips that involved highway travel. Despite my professional role in developing programs and services for elders and caregivers, I was now facing a critically different reality as a family caregiver – everything changes when it’s your own parents.
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