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How to meaningfully reconnect with those who have dementia

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    Thirty years ago,
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    I walked into a nursing home,
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    and my life changed forever.
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    I was there to visit my grandmother Alice.
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    She was a very powerful woman
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    who had lost a battle with a stroke
    that stole her ability to speak.
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    Alice had just three forms
    of communication left.
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    She had this sound
    that was like, "tss, tss, tss,"
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    that she could shift in tone
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    from emphatic, "no, no, no,"
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    to enticing, "yes, you've almost got it."
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    She had an incredibly
    expressive index finger,
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    which she could shake
    and point with frustration.
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    And she had these enormous pale blue eyes
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    that she could open
    and close for emphasis.
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    Wide open seemed to say,
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    "Yes, you've almost got it,"
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    and closing slowly
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    was -- well, it didn't really
    need much translation.
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    It turns out that Alice had taught me
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    that everyone has a story.
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    Everyone has a story.
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    The challenge for the listener
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    is how to invite it into being,
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    and how to really hear it.
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    Now, Alzheimer's and dementia,
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    these are two words that,
    when you say them in front of people,
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    you can watch a cloud descend over them.
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    You can imagine me at dinner parties.
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    "What do you do?"
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    "Well, I invite people with Alzheimer's
    and dementia into expression.
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    Where are you going?"
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    (Laughter)
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    Fear and stigma wrap themselves
    so tightly around an experience
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    that affects 47 million people
    across the world,
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    and they can live with this diagnosis
    for between 10 and 15 years,
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    and that number, 47 million,
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    is supposed to triple by 2050.
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    Family and friends can fade away,
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    because they don't know
    how to be in your company,
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    they don't know what to say,
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    and suddenly,
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    when you need other people the most,
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    you can find yourself
    really painfully alone,
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    unsure of the meaning
    and the value of your own life.
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    Science is pushing for treatments,
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    dreaming of cures,
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    but loosening that grip of stigma and fear
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    could ease the pain
    of so many people right now.
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    And luckily, meaningful connection
    doesn't take a pill.
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    It takes reaching out.
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    It takes listening.
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    And it takes a dose of wonder.
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    That really has become my unending quest,
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    set in motion by Alice
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    and then later on by really
    countless elders in nursing homes
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    and day centers
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    and those struggling to stay at home.
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    And it comes down to the question of how.
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    How do you meaningfully connect?
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    I got a big part of that answer
    from a long-married couple
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    in Milwaukee, Wisconsin, where I'm from,
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    Fran and Jim,
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    whom I met on a rather dreary winter day
    in their tiny, little kitchen
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    in a humble duplex over by Lake Michigan.
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    And when I walked in,
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    Fran and a caregiver and a care manager
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    greeted me really warmly,
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    and Jim stood staring straight ahead,
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    silent.
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    He was on a long,
    slow journey into dementia
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    and was now beyond words.
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    I was there as part of a project team.
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    We were doing what we called
    "artistic house calls,"
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    with a really simple goal
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    of inviting Jim into creative expression,
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    and hopeful in modeling
    for Fran and the caregivers
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    how they could meaningfully connect
    using imagination and wonder.
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    Now, this was going to be no small task,
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    because it turns out
    Jim had not spoken in months.
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    Could he even respond
    if I invited him into expression?
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    I didn't know.
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    Family members, when they try to connect,
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    most commonly will invoke a shared past.
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    We say things like,
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    "Do you remember that time?"
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    But nine times out of 10,
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    the pathway for that one answer
    to travel in the brain is broken,
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    and we're left alone with a loved one
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    in the fog.
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    But there is another way in.
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    I call them beautiful questions.
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    A beautiful question is one
    that opens a shared path of discovery.
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    With no right or wrong answer,
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    a beautiful question helps us
    shift away from the expectation of memory
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    into the freedom of imagination,
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    a thousand possible responses
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    for people with cognitive challenges.
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    Now, back in the kitchen,
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    I did know one thing about Jim.
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    I knew that he liked
    to walk along Lake Michigan,
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    and when I looked around that kitchen,
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    I saw, over by the stove,
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    this trunk that was just covered
    in little pieces of driftwood.
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    And I thought,
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    "I'll try a question
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    that he could answer without words."
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    So I tried,
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    "Jim,
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    can you show me how water moves?"
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    It was silent for a while,
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    but then really slowly he took a step
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    over to that trunk
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    and he picked up a piece of the driftwood
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    and he held it out,
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    and then very slowly
    he began to move his arm,
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    leading with that driftwood.
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    In his hand, it became buoyant,
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    in sync with the motion of the waves
    that he made with his arms.
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    It began this slow journey
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    across calm waters,
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    this gentle rolling to the shore.
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    Transferring his weight
    from left to right and back again,
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    Jim became the waves.
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    His grace and his strength
    just took our breath away.
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    For 20 minutes,
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    he animated one piece
    of driftwood after the other.
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    Suddenly, he was not disabled.
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    We were not gathered in this kitchen
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    for a care crisis.
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    Jim was a master puppeteer,
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    an artist,
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    a dancer.
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    Fran later told me
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    that that moment had been
    a turning point for her,
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    that she learned how to connect with him
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    even as he progressed
    through the dementia.
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    And it really became
    a turning point for me, too.
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    I learned that this creative,
    open-ended approach
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    could help families shift,
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    expand their understanding of dementia
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    as more than just
    tragic emptiness and loss
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    into also meaningful connection
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    and hope
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    and love.
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    Because, creative expression in any form
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    is generative.
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    It helps make beauty and meaning and value
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    where there might have been
    absolutely nothing before.
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    If we can infuse
    that creativity into care,
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    caregivers can invite a partner
    into meaning-making,
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    and in that moment, care,
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    which is so often associated with loss,
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    can become generative.
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    But so many settings of care
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    offer bingo
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    and balloon toss.
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    Activities are passive
    and entertainment-oriented.
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    Elders sit and watch and applaud,
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    really just distracted
    until the next meal.
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    Loved ones trying to keep
    their partners at home
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    sometimes don't have anything to do,
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    and so they resort
    to watching television alone,
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    which compounds the symptoms of dementia
    with what researchers now tell us
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    really are the devastating impacts
    of social isolation and loneliness.
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    But what if meaning-making
    could be accessible
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    to elders and their care partners
    wherever they lived?
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    I've really been totally
    transformed and captivated
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    by bringing these
    creative tools to caregivers
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    and watching that spark
    of joy and connection,
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    discovering that creative play
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    can remind them of why
    they do what they do.
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    Bringing this creative care to scale
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    could truly shift the field.
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    But could we do it?
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    Could we infuse it
    into a whole care organization
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    or an entire care system?
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    The first step towards that goal for me
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    was to assemble a giant team
    of artists and elders and caregivers
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    in one care facility in Milwaukee.
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    Together, over two years,
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    we tackled reimagining the story
    of Homer's "Odyssey."
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    We explored themes.
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    We wrote poems.
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    Together, we created a mile-long weaving.
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    We choreographed original dances.
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    We even explored and learned Ancient Greek
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    with the help of a classics scholar.
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    Hundreds of creative workshops we embedded
    into the daily activities calendar
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    and invited the family members
    to join right along with us,
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    and had caregivers and staff
    from every single area of care
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    collaborating on programming
    for the first time.
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    The culminating moment
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    was an original,
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    professionally produced play
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    that blended the professional performers
    right alongside the elders
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    and the caregivers,
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    and we invited a paying audience
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    to follow us from scene to scene,
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    one in the nursing home,
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    in the assisted living dining room,
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    and finally in the chapel
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    for the final scene
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    where a chorus of elders
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    all playing Penelope
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    lovingly welcomed Odysseus
    and the audience home.
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    Together, we had dared
    to make something beautiful,
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    to invite elders, some with dementia,
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    some on hospice,
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    into making meaning over time,
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    to learn and grow as artists.
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    All this in a place where people
    were dying every day.
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    I find myself now in a place
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    where I'm having to tackle this challenge
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    of meeting a person with dementia
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    across that gap
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    in a more personal way.
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    At a family dinner over the holidays,
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    my mother, who was seated next to me,
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    turned to me and said, "Where's Annie?"
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    My funny and beautiful and feisty mother
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    had been diagnosed with Alzheimer's.
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    And I found myself in that place
    that everyone dreads.
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    She didn't recognize me.
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    And I had to figure out fast
    if I could do what I'd been coaching
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    thousands of other people to do,
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    to connect across that gap.
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    "Do you mean Ellen?" I said,
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    because my sister's empty chair
    was just right across the table from us.
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    "She just went to the bathroom."
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    And my mother looked at me,
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    and then something deep inside sparked,
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    and she reached out and smiled
    and touched my shoulder
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    and she said, "You're right there."
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    And I said, "Yes,
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    I am right here."
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    I know that that moment
    is going to happen again and again,
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    not just for me and my mom
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    but for all 47 million people
    across the world
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    and the hundreds of millions more
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    who love them.
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    How will we answer this challenge
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    that is going to touch the lives
    of every family?
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    How are our care systems
    going to answer that challenge?
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    I hope it is with a beautiful question,
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    one that invites us to find each other
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    and connect.
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    I hope our answer
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    is that we value care
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    and that care can be generative
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    and beautiful.
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    And that care can put us in touch
    with the deepest parts of our humanity,
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    our yearning to connect
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    and make meaning together
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    all the way to the end.
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    Thank you.
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    (Applause)
Title:
How to meaningfully reconnect with those who have dementia
Speaker:
Anne Basting
Description:

By incorporating art and creativity into elder care settings, gerontologist Anne Basting helps families reconnect with loved ones who have dementia. In this moving talk, she shares how asking "beautiful questions" -- questions that don't have a right or wrong answer -- opens up a shared path of discovery, imagination and wonder. "If we can infuse creativity into care, caregivers can invite a partner into meaning-making," Basting says. "In that moment, care, which is so often associated with loss, can become generative."

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Video Language:
English
Team:
closed TED
Project:
TEDTalks
Duration:
14:38

English subtitles

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