There are two common operational practices that make it difficult for organizations to visualize a pathway to unlocking doors (and many other activities as well): all-or-none thinking and surplus safety. I explore each of these in the conclusion to my series “Hidden Restraints.”
Recently, I posted a provocative argument for considering locked doors as physical restraints. I have received many comments about the post; and as promised, I am following up with a second installment (of three), in which I will give some guidelines for those who wish to take up the challenge.
New research validates what we already know — the use of antipsychotic medications to reduce behavioral and psychological symptoms of dementia (BPSD) is not very effective and what we should be doing instead is focusing on meeting the unmet needs of the person living with dementia through person centered approaches.
The Alzheimer’s Family Support Center of Cape Cod is a non-profit organization designed to be age- and dementia-friendly, which means that the programs are organized in a way that enables individuals of all ages and disease states to participate in the program.
We know what the experience of Alzheimer’s looks like from the outside and its correlation with age is undeniable. We do not know the exact culprit, or combination of culprits, of these experiences; therefore, classing it as a disease to be eradicated is to put the proverbial cart before the horse.
While Alzheimer’s creates challenges for those who live with it – and for their loved ones who watch them endure it – dementia should never define a person, or lead them to believe they ought to just give up and submit to it.
Subscriber’s to the late Richard Taylor’s e-newsletter Alzheimer’s From the Inside Out had the bittersweet privilege of receiving his last email yesterday with a forward from his brother Jason.
I have decided to coin a new philosophy around the support of people who live with changing cognitive abilities.
This short and not-too-sweet post is an addendum to my guest editorial that was published here in McKnight’s on Friday, July 24th.
“Hello. My name is Richard, and I have dementia, probably of the Alzheimer’s type.” These are the words Dr. Richard Taylor used to open each of his presentations, as he enlightened the world about the lived experience of changing cognitive ability. Richard passed away at his home on July 25th, due to cancer.
Last week I came across the most irresponsible, ill-informed, and inflammatory bit of writing I have ever seen on the topic of dementia.
I believe our top priority is to build all inclusive communities, both for our aging population in general, as well as those living with changing cognitive abilities of all kinds. Here’s why: