Category: Alzheimer’s Association Dallas

Caregiver’s Log, October 13, 2017

by Samra Jones Bufkins I’m going to start “Caregiver Logs” (inspired by Star Trek’s Captain’s Log) as part of this blog, describing incidents and behaviors we experience. For the first few posts I’ll be going back in recent time. I’ll venture into the TMI zone here, because people need to know that hostility, agitation and … Continue reading Caregiver’s Log, October 13, 2017

Challenging the Alzheimer’s Association to make “The Longest Day” relevant

"The Longest Day" should be a day of service. I've been a big supporter of the Alzheimer's Association, but frankly, I'm a little tired of the emphasis on "awareness" and the importance of fundraising. I'm ready for action.

Ambiguity and turning 60

Ambiguity and turning 60

There’s a term for one of the feelings caregivers suffer while their loved one is still alive—Ambiguous Loss.* Caregivers for people with dementia suffer the painful paradox of living with a person who is physically present but sometimes psychologically absent. The rollercoaster ride of good days and bad days exacerbates the ambiguity of the loss.

It’s The Little Things….

August 13, 2013 By Samra Jones Bufkins I think of that Robert Earl Keen song every time I remember "It's the little things." Of course, his song addresses completely different issues, but you get the idea, especially when you hear the last line of the chorus. And dealing with dementia means the little things add up. Original image from … Continue reading It’s The Little Things….

The Less He Remembers, the More I Know

On Tuesday we ventured back down to UTSW Medical School in Dallas, specifically to the Memory Clinic, for another evaluation for Bill.  A year ago when we made this trip he drove, and I was holding out hope the problems with his memory and confusion were normal pressure hydrocephalus. After an MRI, blood tests, neuropsychological testing and a thorough evaluation … Continue reading The Less He Remembers, the More I Know