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:
I promised to follow-up with additional blog posts about my experience at the Alzheimer’s Disease International 2015 conference in Perth, Western Australia. Here is a quick post with full video from my plenary session.
People living with various forms of dementia often exhibit certain signs of emotional upset, which may include anger, sadness, fear, frustration, or anxiety. Have any of you ever experienced these feelings? Maybe you too have dementia!
America has a looming public health crisis. And it also happens to be America’s favorite pastime.
Sometimes we need to be reminded we are on a journey and an illness does not define who we truly are.
Prepare your brain for a bountiful flood of new research on how music can “Change the Brain.”
Yesterday I had a conversation with the Quality Improvement Organization (QIO) in my home state of Montana about how to change dementia caregiving practices in the state’s nursing homes. I offered three ideas and would like suggestions from readers.
Beyond awareness, we need to develop comprehensive, personalized brain health strategies that gradually modify our behaviors, replacing risky behaviors and habits with ones that protect and strengthen the brain.
Monday’s New York Times article “Complexities of Choosing an End Game for Dementia” provides a good opportunity to reflect on the complex ethical questions surrounding dementia.
Given the reality that most people are not currently equipped with the knowledge and resources to implement other solutions, there will be times when the use of medication may need to be considered. So here are some guidelines for those along the journey who have not yet created the infrastructure for an anti-psychotic-free environment.
Have you watched Alive Inside yet? It’s available on DVD and streaming on Netflix. Let’s put music at the heart of the conversation about what makes a life worth living.
Recently, a friend who works in long-term care wrote to ask if I had any formal guidelines for prescribing antipsychotic drugs to people living with dementia.
Recently, I was interviewed for an article at Chabad.org about tips for including loved ones living with dementia in Chanukah celebrations. With Christmas fast approaching, it seems appropriate to review a few of those tips here for your upcoming family gatherings.
One of the nicest compliments I ever received for my work came in an unexpected way; in fact, I had to think about it for a while to decide if it truly was a compliment.
Thanks to NPR for identifying this ongoing issue, but we need to also broaden the discussion to look at how our society views dementia, how we have chosen to care for our elders, and the systems that regulate and reimburse that care.
If you are in the mood for a slapped together blog post that is simultaneously alarmist and deeply pessimistic you might want to read Ken Dychtwald’s recent piece on Huffington Post for Alzheimer’s Disease Awareness Month.
I have been advocating that community planners switch to the terms “age-inclusive” and “dementia-inclusive,” as these terms raise the bar by requiring the inclusion of such people in all aspects of community life and planning, rather than simply creating a kind but misguided process of substituted judgment.
We have been graphing the age and dementia distribution for baby boomers for decades, and yet none of our projections have ever extended beyond the year 2050. Why is that?
I recently cautioned in an op-ed that our attempts to reduce antipsychotic drugs among patients with dementia would soon become problematic if we have not also learned how to care differently. And the chickens are starting to come home to roost.