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The Missoula Demonstration Project We're Setting an Example for Others
Recently, at a small dinner in New
York with health care researchers, someone asked why I live in Missoula, "of
all places". I usually respond to such questions by talking about the
beauty of Montana and about the quality of life here. On this evening, a
colleague who has been here and loves Missoula, pitched in, "When the plane lands in Missoula, the captain
announces there's been a time change and suggests that
passengers reset their watches to 1955." I had to grin and bear ribbing about living in Mayberry, replete
with images of Aunt Bea's lemonade, porch swings and bandshell
concerts.
Timing is everything. Once the
chuckles subsided, I pointed out that life in the Garden City is better than
the bucolic image of 1955. Besides porch swings, the Carousel, Farmers Market
and Out to Lunch, we have reliable air service (well mostly), cable and
satellite TV and, of course, the Internet. Missoulians are active nationally
and internationally. My colleagues' big-city smugness visibly dampened. But I
wasn't
finished yet.
By the time our salads arrived, the
conversation had turned to our collective worry about the future of American
health care. Major social and demographic trends are already resulting in a
tidal wave of caregiving need. As the baby boomers age, for the first time
there will be more older people than younger people on the planet. Half of
everyone who has ever lived to be 65 years old is alive today! Adding to the challenge is chronic illness, "an
invention"
of the latter half
of the 20th Century. Medicine enables people to live for years with
diseases that formerly caused death abruptly, but also precipitates
unprecedented social dilemmas.
The mood during our main course was somber as we
realized that every one of us was currently dealing with a grandparent, parent
or in-law who either needs care at present, or is frail, perhaps at risk of
falling, or otherwise soon to be in need of home health or residential care.
We Americans are finding it hard to
adequately care for the people we love. Many of us are part of two-job couples
and live a great distance from our parents. We all want our mothers and
fathers to have "the best
care possible," but even
those of us who are doctors and nurses are frustrated by how hard it is to
access basic services. Many of us are in the "sandwich generation," not finished with child rearing but inexorably
drawn into parent care. Our siblings and friends help when they can, but
peoples' time and capacity are limited.
These social problems are being
played out in every community. Indeed, how we will care for the soaring
numbers of ill, infirm and advanced elderly among us will be the central
social and moral questions confronting the baby boom generation.
Dessert arrived and we began to focus on hopeful strategies. I pointed out that
people who live in Missoula are also dealing with these problems. But Missoula
is unique in one respect. As a community we are confronting these issues
head-on. Hundreds of Missoulians have built the Missoula Demonstration Project
to be a community-based vehicle with which to grapple with these profound
challenges.
Under the auspices of the Missoula
Demonstration Project, people from many walks of life are working to improve the
quality of life's end. Task
forces are raising awareness and skills related to pain management and advance
care planning. Others are exploring how best to integrate the realities of
dying, caregiving and grief within the life our faith communities, workplace
communities, schools, clubs and neighborhoods. The Project=s Life Stories task force has given rise to StoryKeepers, Inc. a new
community-based, non-profit organization dedicated to helping people review and
record their personal histories. Through the Arts task force Missoulians have
learned to create memorials for loved ones who have died.
The Missoula Demonstration Project
doesn't come with a fixed
vision or set of answers. The more we learn, the clearer it becomes that we will
have to live out our collective response to the challenges of dying, caregiving
and grieving. The Project can,
however, offer its research to foster quality improvement on a community-wide
basis. We can align what we value and hope for with how we care for and support
one another. The opportunities are limited only by our imagination and
commitment. "You're really doing all that in
Missoula?", one
colleague, now wide-eyed inquired. We really are. Of course, there are cynics
who roll their eyes and scoff at this pie-in-the-sky notion. It is, afterall,
So Missoula!
Yes it is. Our willingness to live in
community B rather than merely in proximity B with one another enriches
the quality of life here, just as much as our mountains and streams. Missoulians
are the main beneficiaries, but our community's efforts will also shed
light on what communities elsewhere can do.
Even the most skeptical of locals will benefit from these efforts. Missoula may not be Mayberry but
together we are making it an ever-better place to grow up, grow old and grow on.
By the time the bill arrived, several colleagues
who had poked fun at the notion of living in Missoula asked me when they might
come for a visit. In the process of caring for ourselves, we are already setting
an example from which others can learn.
Ira Byock, MD, is the co-founder and principal investigator for the
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