Not Alzheimer's?
Our services are also for these related disorders.

Alzheimer's Association, New York City Chapter

  • 24-hour helpline: 800.272.3900
  • Translation available in 140 languages
  • Click here to contact us

 

Search
 
Select a Topic
Newsletter Home
Front Page
The Melting Pot
President's Message
From the
Program Director
From the Editor's Desk
Early-Stage Memory Disorders Forum
Five Questions For
Anne Basting
Early-Stage Services
Demolition Derby
MedicAlert + Safe Return
Della's Space
Helpline Update
Go Direct
Diversity &
Outreach Updates
Caregivers' Corner
If It's Not Alzheimer's ...
Normal Pressure Hydrocephalus
A Reason To Celebrate!
In Our Own Words
1st Annual Nursing
Home Conference
4th Annual
Caregiver Soirée
Reflections - Part 2
Dr. Mony de Leon
Public Policy Update
Legal Guidance
Access to Health Care for Uninsured Immigrants
City-Wide Immigrant Caregiver Program
Volunteer Corner
Research Study
Junior Committee Update
Women In Action
Ways To Give
Naming Opportunities
Development Report
Donor Profiles
Tributes
N.Y.C.A.R.E.
Inhibiting RAGE: A New Way to Treat Alzheimer Disease?
Clinical Trials
Columbia University Clinical Trials
NYU Clinical Trials
Mt. Sinai Clinical Trials
Point of View
ALZNYC Store
Bulletin Board
Know Your Charity
HonorGift Tribute Cards
Chapter Staff
Board of Directors
Education Calendar
Support Groups

En Español
Archived Versions
Featured Articles Index
 
 
   
   
 
 
Text Size A  A  A


1. Can you tell us a little bit about yourself?

I’m trained as both an artist (writer) and a cultural critic. I started studying and writing about aging in my undergraduate creative writing classes at Colorado College. People often ask me how I got interested in aging – as though it’s a strange obsession. I think it’s perfectly normal for a young person to think about things like the meaning and limits of life. But I do try to give an honest answer. As best I can figure (and my parents confirm), I was a kid who got along better with adults – which means I probably didn’t have many friends my own age. During my junior high school years I took art classes outside of school and most of the other students were retired people. My grandmother and I were very close as well. When I was in college I spent a month in Chicago studying Shakespeare at the Newberry Library. While I hung out with my fellow students at the blues bars, I also relished the company of my grandmother’s best friend. We had a fabulous time going out for dinner and drinking strawberry daiquiris.

All of my graduate studies (University of Wisconsin- Madison and University of Minnesota) focused on social performance of aging. I also kept writing and producing plays during those five years.

Currently I am the director of the Center on Age and Community, and associate professor of Theatre at the Peck School of the Arts, University of Wisconsin-Milwaukee. I now live in Milwaukee with my two boys, Ben, age 6, and Will, age 3, and my husband Brad Lichtenstein, who is a documentary filmmaker, and a reluctant transplant from New York. We still own our house in Brooklyn’s Lefferts Manor.

2. What motivated you to apply your talent and training to working with people with Alzheimer’s disease and related dementias?

After graduating with my Ph.D., I was lucky to receive a Rockefeller Fellowship to turn my dissertation into a book. This became, in 1998, The Stages of Age: Performing Age in Contemporary American Culture. It basically says that playing a new role (quite literally on stage, or in everyday life) can change the prevailing attitudes about aging – that aging necessarily entails a growing rigidity, decline, or inability to change. I started getting interested in whether people with dementia could experience the same transformation through performance that healthy older adults clearly did. And that’s when I started experimenting with the role of artist and storyteller for people with dementia.

3. You have achieved considerable recognition for your very creative TimeSlips program. Can you briefly describe this program and tell us what inspired its development?

Thank you for saying so…it’s hard to believe that the project started 10 years ago and today it has 11 training bases across the country. TimeSlips was born out of frustration. I was volunteering at a nursing home to see if some of the creative drama exercises that clearly benefited cognitively healthy older adults could benefit people with cognitive disabilities. I tried lots of reminiscence-type of exercises and nothing was working. It was a very rough scenario though – a chaotic day room and people who were clearly, shall we say, pharmaceutically restrained. I’d been trying to make something work, to play with the group a bit, for six weeks and nothing was happening. One day I decided to drop all reference to memory and see if they responded better to making things up. I brought in an image and asked them to make up a new story together. To my great shock (and the staff ’s as well I should add), we told an elaborate story for about 40 minutes. We sang and laughed. Clearly, they were transformed by the role of storyteller – not of individual memories, but of a shared effort at weaving a new tale from their collective imaginations. After that day, I just kept trying to replicate the magic of that first session. And I’ve been trying to replicate it, and teach others to do the same, for 10 years now.

4. How did you become involved with StoryCorps and the Memory Loss Initiative? Do you see a connection between the goals of TimeSlips and this program?

The second I heard about the StoryCorps project, I called the founder, Dave Isay, and asked him if he was training his facilitators to understand memory loss – because surely, people who feel their memories threatened would be eager, if not first in line, to capture them on disc. The idea for StoryCorps was so simple, so brilliant, so needed, that it has swept away Isay into one of the fastest growing non-profits in the country. He couldn’t entertain the issue of memory loss in 2003 – too much was happening. But in 2005, we talked again. He had a potential funder who was interested in addressing memory loss. And we wrote a proposal to do a pilot year – training StoryCorps facilitators, creating guidelines for memory loss interviews, and reaching out to people with memory loss to encourage them to try StoryCorps. It’s a fantastic project. TimeSlips is more focused on the imagination, and on group storytelling, but many of the same communication techniques are at the core of both programs. Both programs are eager to share the stories that emerge to raise awareness about the creativity, humanity, and capacity of people with dementia.

5. Based on your successful experience with creative pursuits for people with progressive memory disorders, is there any message you have for the audience who will be attending the 8th Annual Early-Stage Memory Disorders Forum? Would you encourage people to find a way to preserve their life stories?

When people hear the word “dementia,” they think decline and loss. They don’t tend to think of growth. The last 10 years of my life have been spent trying to teach people that growth and loss aren’t mutually exclusive. Dementia certainly entails some loss of ability with language, even in the early stage, but there are so many other ways to express one’s self. Creativity and the arts can open up a whole new world to people with a progressive memory disorder. They offer a way to make meaning, leave legacy, and connect with friends, care partners, and future generations. They offer a way to grow.

 

Previous | Next

 
 
 
  Donate | About this Site | Security | Privacy Policy | Disclaimer | Staff Login


igive
up to 26% of your next online purchase can go towards ALZNYC
Wise Giving Alliance Standard
Seal of Approval