The first rule of any debate, or “heated” discussion, is to know your definitions. If you don’t, not much else matters. With caregiving, it comes down to knowing your people.
Do you really want to know when you’ll get Alzheimer’s?
By
John O'Connor
Mar 14, 2014
Sometimes, ignorance truly is bliss. Or at least, it’s better than what’s waiting around the corner. Soon, researchers say, we might be able to learn if we’re going to get Alzheimer’s...
Genetic testing opens can of worms for Alzheimer’s patients
By
Elizabeth Newman
Mar 25, 2015
Healthcare professionals tend to have a belief in facts, and as a corollary believe in conventional wisdom that knowledge is power. Of course, what people SAY they want to know and how they actually act...
Glen Campbell Alzheimer’s documentary brings out the stars — caregivers and celebrities alike
By
James M. Berklan
Oct 22, 2014
As readers of this blog may recall, my expectations for the special screening of the new documentary about music superstar Glen Campbell’s journey with Alzheimer’s disease were high. Sunday...
Gender adjustments for Alzheimer’s caregivers
By
Allan S. Vann, Ed.D
Jan 10, 2014
For quite some time, I was the only male in my Alzheimer’s disease spousal support group. I quickly discovered that I could not resolve some problems for my wife, Clare, in the same way as some women...
‘The Best Days’ — a best read
By
James M. Berklan
Apr 02, 2014
Where to start when discussing Jean Rene Champion’s engrossing memoir is a difficult question, rivaled only by the struggle of where to stop. His self-published “The Best Days of My Life: Memories...